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Asymmetric Catalysis Mediated by Synthetic Peptides

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Outgoing claims: the papers this work cites, builds on, or argues with.

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De novo designed polypeptide catalysts with adopted folded structures

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Preparation of polyamino acid catalysts for use in Juli� asymmetric epoxidation

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The Catalytic Asymmetric Aldol Reaction

inferredcites →https://doi.org/10.1002/1099-0690(200206)2002:12<1877::aid-ejoc1877>3.0.co;2-uopenalex-snapshot

Asymmetric Michael Additions to Nitroalkenes

inferredcites →https://doi.org/10.1002/1521-3765(20000616)6:12<2214::aid-chem2214>3.0.co;2-eopenalex-snapshot

Reactive-Site Design in Folded-Polypeptide Catalysts-The Leaving Group pKa of Reactive Esters Sets the Stage for Cooperativity in Nucleophilic and General-Acid Catalysis

inferredcites →https://doi.org/10.1002/1521-3765(20020104)8:1<84::aid-chem84>3.0.co;2-nopenalex-snapshot

Nitroxyl Peptides as Catalysts of Enantioselective Oxidations

inferredcites →https://doi.org/10.1002/1521-3773(20001016)39:20<3635::aid-anie3635>3.0.co;2-yopenalex-snapshot

Asymmetric Conjugate Addition of Azide toα,β-Unsaturated Carbonyl Compounds Catalyzed by Simple Peptides

inferredcites →https://doi.org/10.1002/1521-3773(20010803)40:15<2824::aid-anie2824>3.0.co;2-jopenalex-snapshot

Incorporation of Peptide Isosteres into Enantioselective Peptide-Based Catalysts as Mechanistic Probes

inferredcites →https://doi.org/10.1002/adsc.200404070openalex-snapshot

Esterolytic Peptide Dendrimers with a Hydrophobic Core and Catalytic Residues at the Surface

inferredcites →https://doi.org/10.1002/adsc.200505373openalex-snapshot

Small Peptide‐Catalyzed Enantioselective Addition of Ketones to Nitroolefins

inferredcites →https://doi.org/10.1002/anie.196510792openalex-snapshot

Stereospecific Synthesis of D ‐Hydroxynitriles and Optically Active Ethanolamines

inferredcites →https://doi.org/10.1002/anie.197902393openalex-snapshot

Methods of Reactivity Umpolung

inferredcites →https://doi.org/10.1002/anie.198009291openalex-snapshot

“Synthetic Enzymes”. Highly Stereoselective Epoxidation of Chalcone in a Triphasic Toluene‐Water‐Poly[(S)‐alanine] System

inferredcites →https://doi.org/10.1002/anie.198307951openalex-snapshot

Preparation of 2‐(1‐Hydroxyalkyl)acrylic Esters; Simple Three‐Step Synthesis of Mikanecic Acid

inferredcites →https://doi.org/10.1002/anie.200250422openalex-snapshot

Catalyst–Substrate Coimmobilization: A Strategy for Catalysts Discovery in Split‐and‐Mix Libraries

inferredcites →https://doi.org/10.1002/anie.200301686openalex-snapshot

Recent Developments in the Catalytic Asymmetric Cyanation of Ketimines

inferredcites →https://doi.org/10.1002/anie.200390354openalex-snapshot

Catalytic Peptide Dendrimers

inferredcites →https://doi.org/10.1002/anie.200460177openalex-snapshot

A Combinatorial Approach to Catalytic Peptide Dendrimers

inferredcites →https://doi.org/10.1002/anie.200601490openalex-snapshot

Site‐Selective Derivatization and Remodeling of Erythromycin A by Using Simple Peptide‐Based Chiral Catalysts

inferredcites →https://doi.org/10.1002/bip.20356openalex-snapshot

Cα‐Tetrasubstituted amino acid based peptides in asymmetric catalysis

inferredcites →https://doi.org/10.1002/bip.20373openalex-snapshot

Oligopeptides as catalysts for asymmetric epoxidation

inferredcites →https://doi.org/10.1002/bip.20393openalex-snapshot

Solid‐supported and pegylated H–Pro–Pro–Asp–NHR as catalysts for asymmetric aldol reactions

inferredcites →https://doi.org/10.1002/bip.20394openalex-snapshot

Combinatorial synthesis, selection, and properties of esterase peptide dendrimers

inferredcites →https://doi.org/10.1002/bip.20413openalex-snapshot

Asymmetric enone epoxidation by short solid‐phase bound peptides: Further evidence for catalyst helicity and catalytic activity of individual peptide strands

inferredcites →https://doi.org/10.1002/chem.200400160openalex-snapshot

De novo Metallonucleases Based on Helix–Loop–Helix Motifs

inferredcites →https://doi.org/10.1002/chem.200500139openalex-snapshot

Amino Acid Catalyzed Neogenesis of Carbohydrates: A Plausible Ancient Transformation

inferredcites →https://doi.org/10.1002/chem.200501639openalex-snapshot

Direct Asymmetric Intermolecular Aldol Reactions Catalyzed by Amino Acids and Small Peptides

inferredcites →https://doi.org/10.1002/ejoc.200400243openalex-snapshot

Trends in Asymmetric Michael Reactions Catalysed by Tripeptides in Combination with an Achiral Additive in Different Solvents

inferredcites →https://doi.org/10.1002/ejoc.200500044openalex-snapshot

Investigation of Diketopiperazines Containing a Guanidino‐Functionalized Sidechain as Potential Catalysts of Enantioselective Strecker Reactions

inferredcites →https://doi.org/10.1002/jlac.18500750103openalex-snapshot

Ueber die künstliche Bildung der Milchsäure und einen neuen, dem Glycocoll homologen Körper;

inferredcites →https://doi.org/10.1002/macp.1968.021120107openalex-snapshot

Synthesis of optically active polymers by asymmetric catalysts. VIII. Asymmetric polyaddition of dimercaptan to dimethacrylate by optically active amine as catalyst

inferredcites →https://doi.org/10.1002/macp.1971.021500109openalex-snapshot

Asymmetric addition catalyzed by optically active polymers. II.

inferredcites →https://doi.org/10.1002/macp.1972.021600105openalex-snapshot

Asymmetric addition catalyzed by optically active polymers. III.

inferredcites →https://doi.org/10.1002/macp.1975.021760923openalex-snapshot

Asymmetric synthesis catalyzed by poly(5‐benzyl L ‐glutamate)

inferredcites →https://doi.org/10.1002/macp.1975.021761208openalex-snapshot

Asymmetric synthesis catalyzed by poly(4‐benzyl L ‐aspartate)

inferredcites →https://doi.org/10.1002/macp.1976.021770904openalex-snapshot

Effect of ethanol on the asymmetric synthesis catalyzed by poly(5‐benzyl L ‐glutamate) and poly(4‐benzyl L ‐aspartate)

inferredcites →https://doi.org/10.1002/macp.1976.021771001openalex-snapshot

Asymmetric synthesis catalyzed by poly‐ L ‐alanine

inferredcites →https://doi.org/10.1002/macp.1977.021780123openalex-snapshot

Asymmetric addition of 1‐dodecanethiol to isopropenyl methyl ketone catalyzed by poly(α‐amino acid)s: Determination of the enantiomeric purity of the product

inferredcites →https://doi.org/10.1002/macp.1977.021780209openalex-snapshot

Asymmetric synthesis catalyzed by (S)‐alanine‐N‐propylamide as a terminal model of poly[(S)‐alanine]

inferredcites →https://doi.org/10.1002/macp.1978.021790403openalex-snapshot

Asymmetric synthesis catalyzed by oligo((S)‐alanine)

inferredcites →https://doi.org/10.1002/macp.1978.021791202openalex-snapshot

Polycondensation d'acides α‐aminés par des systèmes iode‐phosphites en présence de pyridine ou d'imidazole

inferredcites →https://doi.org/10.1002/macp.1979.021800431openalex-snapshot

Asymmetric cyanohydrin synthesis catalyzed by synthetic dipeptides, 1

inferredcites →https://doi.org/10.1002/macp.1979.021800601openalex-snapshot

Asymmetric synthesis catalyzed by poly(α‐amino acid)s with a tertiary amino end group

inferredcites →https://doi.org/10.1002/macp.1982.021830307openalex-snapshot

Asymmetric cyanohydrin synthesis catalyzed by synthetic dipeptides, 2

inferredcites →https://doi.org/10.1002/macp.1985.021860903openalex-snapshot

Asymmetric addition of hydrogen cyanide to aliphatic aldehydes catalyzed by a synthetic cyclic peptide, cyclo[(S)‐phenylalanyl‐(S)‐histidyl]

inferredcites →https://doi.org/10.1002/marc.1996.030170206openalex-snapshot

The role of the membrane‐assisted hydrophobic interaction between di‐, tri‐, or tetrapeptide catalysts and amino acid esters for the enhancement of stereoselective hydrolysis reactions

inferredcites →https://doi.org/10.1002/qsar.200540009openalex-snapshot

Using Catalyst-Substrate Coimmobilization for the Discovery of Catalysts for Asymmetric Aldol Reactions in Split-and-Mix Libraries

inferredcites →https://doi.org/10.1007/3-540-48990-8_2openalex-snapshot

Functionalization and Properties of Designed Folded Polypeptides

inferredcites →https://doi.org/10.1007/bf01732950openalex-snapshot

β-structures of polypeptides with L- and D-residues

inferredcites →https://doi.org/10.1007/bf01808274openalex-snapshot

Chemical activity of simple basic peptides

inferredcites →https://doi.org/10.1016/0008-6215(92)85043-yopenalex-snapshot

Lewis acid-catalysed rearrangements of myo-inositol orthoformate derivatives

inferredcites →https://doi.org/10.1016/0040-4039(95)00317-6openalex-snapshot

General synthesis of phosphatidylinositol 3-phosphates

inferredcites →https://doi.org/10.1016/0040-4039(95)01967-mopenalex-snapshot

Serine proteinases mimics: hydrolytic activity of cyclic peptides which include a non-natural amino acid

inferredcites →https://doi.org/10.1016/0040-4039(96)00590-4openalex-snapshot

A remarkably enhanced diastereoselectivity for the hydrolysis of dipeptide esters responding to pH and temperature in buffer solutions

inferredcites →https://doi.org/10.1016/0304-5102(83)80109-6openalex-snapshot

Isokinetic relationships for the enantioselective deacylation of p-nitrophenyl N-acylphenylalanates in bilayer and micellar systems

inferredcites →https://doi.org/10.1016/0957-4166(92)80019-sopenalex-snapshot

Polymer attached cyclic dipeptides as catalysts for enantioselective cyanohydrin formation

inferredcites →https://doi.org/10.1016/0957-4166(95)00239-lopenalex-snapshot

The catalytically active conformation of cyclo-[(S)-His-(S)-Phe] as determined by solid state NMR

inferredcites →https://doi.org/10.1016/0957-4166(96)00089-4openalex-snapshot

Asymmetric hydrocyanation of aldehydes with cyclo-dipeptides: A new mechanistic approach

inferredcites →https://doi.org/10.1016/j.cbpa.2005.10.013openalex-snapshot

Dendrimers as artificial enzymes

inferredcites →https://doi.org/10.1016/j.tet.2003.05.002openalex-snapshot

A peptide-based catalyst approach to regioselective functionalization of carbohydrates

inferredcites →https://doi.org/10.1016/j.tet.2006.01.104openalex-snapshot

Dihedral angle restriction within a peptide-based tertiary alcohol kinetic resolution catalyst

inferredcites →https://doi.org/10.1016/j.tet.2006.05.005openalex-snapshot

Amino acid-peptide-catalyzed enantioselective Morita–Baylis–Hillman reactions

inferredcites →https://doi.org/10.1016/j.tetasy.2004.06.046openalex-snapshot

Enantioselective epoxidation of chalcone catalysed by the artificial enzyme poly-l-leucine: kinetic mechanism

inferredcites →https://doi.org/10.1016/j.tetasy.2005.04.027openalex-snapshot

(S)-Histidine-based dipeptides as organic catalysts for direct asymmetric aldol reactions

inferredcites →https://doi.org/10.1016/j.tetasy.2005.06.031openalex-snapshot

Heterogeneous catalysis of the asymmetric aldol reaction by solid-supported proline-terminated peptides

inferredcites →https://doi.org/10.1016/j.tetasy.2006.03.012openalex-snapshot

4-trans-Amino-proline based di- and tetrapeptides as organic catalysts for asymmetric C–C bond formation reactions

inferredcites →https://doi.org/10.1016/j.tetlet.2004.03.120openalex-snapshot

Structure and catalytic activity of some soluble polyethylene glycol–peptide conjugates

inferredcites →https://doi.org/10.1016/j.tetlet.2004.04.188openalex-snapshot

Novel conditions for the Juliá–Colonna epoxidation reaction providing efficient access to chiral, nonracemic epoxides

inferredcites →https://doi.org/10.1016/j.tetlet.2004.04.189openalex-snapshot

Scoping the triphasic/PTC conditions for the Juliá–Colonna epoxidation reaction

inferredcites →https://doi.org/10.1016/j.tetlet.2004.04.190openalex-snapshot

Asymmetric epoxidation of some arylalkenyl sulfones using a modified Juliá–Colonna procedure

inferredcites →https://doi.org/10.1016/j.tetlet.2005.06.096openalex-snapshot

Asymmetric epoxidation of α,β-unsaturated ketones catalyzed by silica-grafted poly-(l)-leucine catalysts

inferredcites →https://doi.org/10.1016/j.tetlet.2005.09.113openalex-snapshot

Direct asymmetric aldol reaction in aqueous media using polymer-supported peptide

inferredcites →https://doi.org/10.1016/j.tetlet.2007.01.073openalex-snapshot

Asymmetric Michael addition of α-nitro-ketones using catalytic peptides

inferredcites →https://doi.org/10.1016/s0040-4020(01)80840-1openalex-snapshot

Recent developments in the stereoselective synthesis of α-aminoacids

inferredcites →https://doi.org/10.1016/s0040-4020(01)82043-3openalex-snapshot

Enantioselective synthesis of flavonoids. Part 1. Poly-Oxygenated chalcone epoxides

inferredcites →https://doi.org/10.1016/s0040-4020(01)86778-8openalex-snapshot

Enantioselective synthesis of flavonoids. Part 2. Poly-oxygenated α-hydroxydihydrochalcones and circular dichroic assessment of their absolute configuration

inferredcites →https://doi.org/10.1016/s0040-4020(01)88574-4openalex-snapshot

Synthetic enzymes—4

inferredcites →https://doi.org/10.1016/s0040-4020(01)91272-4openalex-snapshot

Asymmetric epoxidation of electron-poor olefins-V

inferredcites →https://doi.org/10.1016/s0040-4020(02)00516-1openalex-snapshot

Proline-catalyzed asymmetric reactions

inferredcites →https://doi.org/10.1016/s0040-4039(00)00465-2openalex-snapshot

Concise syntheses of l-α-phosphatidyl-d-myo-inositol 3-phosphate (3-PIP), 5-phosphate (5-PIP), and 3,5-bisphosphate (3,5-PIP2)

inferredcites →https://doi.org/10.1016/s0040-4039(00)84211-2openalex-snapshot

Enantioselective and diastereoselective cleavage of amino acid esters in coaggregates of controlled size

inferredcites →https://doi.org/10.1016/s0040-4039(00)84576-1openalex-snapshot

Diastereoselective synthesis of (E)-alkenes and (E)-1,ω-dienes starting from diastereoisomeric mixtures of 1-bromo-1-alkenes: New syntheses of monounsaturated or bridged ring-ketal naturally occurring substances.

inferredcites →https://doi.org/10.1016/s0040-4039(00)87240-8openalex-snapshot

Stereoselectivity in micellar and vesicular reactions

inferredcites →https://doi.org/10.1016/s0040-4039(00)92379-7openalex-snapshot

Synthesis and characterization of cyclic peptides with hydrolytic activity

inferredcites →https://doi.org/10.1016/s0040-4039(00)96644-9openalex-snapshot

The first enantioselective synthesis of poly-oxygenated α-hydroxydihydrochalcones and circular dichroic assessment of their absolute configuration

inferredcites →https://doi.org/10.1016/s0040-4039(00)98064-xopenalex-snapshot

A remarkable steric control for the enantioselective hydrolytic-cleavage of amino acid esters responding to ionic strength

inferredcites →https://doi.org/10.1016/s0040-4039(01)00535-4openalex-snapshot

Asymmetric epoxidation of a geminally-disubstituted and some trisubstituted enones catalysed by poly-l-leucine

inferredcites →https://doi.org/10.1016/s0040-4039(01)80158-1openalex-snapshot

Isokinetic discrimination of artificial membrane systems in the enantioselective hydrolysis

inferredcites →https://doi.org/10.1016/s0040-4039(01)82904-xopenalex-snapshot

Mechanistic alteration in micellar peptide esterolysis reactions

inferredcites →https://doi.org/10.1016/s0040-4039(01)83371-2openalex-snapshot

New amino acid-functionalized surfactants; preparation and catalytic properties

inferredcites →https://doi.org/10.1016/s0040-4039(01)85318-1openalex-snapshot

A cysteine-functionalized micellar catalyst

inferredcites →https://doi.org/10.1016/s0040-4039(01)86340-1openalex-snapshot

Enantioselectively catalyzed hydrolysis of p-nitrophenyl esters of N-protected L-amino acids by N-lauroyl L or D-histidine in CTABr micelles.

inferredcites →https://doi.org/10.1016/s0040-4039(03)00666-xopenalex-snapshot

Hole transfer in DNA: DNA as a scaffold for hole transfer between two organic molecules

inferredcites →https://doi.org/10.1016/s0040-4039(98)01249-0openalex-snapshot

Synthesis of optically active 2,3-substituted-1,2,3,4-tetrahydro-4-quinolones using polyleucine

inferredcites →https://doi.org/10.1016/s0040-4039(98)02090-5openalex-snapshot

Towards a mechanistic insight into the Juliá-Colonna asymmetric epoxidation of α,β-unsaturated ketones using discrete lengths of poly-leucine

inferredcites →https://doi.org/10.1016/s0040-4039(98)02689-6openalex-snapshot

Overcoming intrinsic diastereoselection using polyleucine as a chiral epoxidation catalyst

inferredcites →https://doi.org/10.1016/s0040-4039(99)00129-xopenalex-snapshot

Steric-control for the enantioselective hydrolysis of amino acid esters with membrane-bound enzyme models

inferredcites →https://doi.org/10.1016/s0040-4039(99)01021-7openalex-snapshot

Polyamino acid-catalysed asymmetric epoxidation: Sodium percarbonate as a source of base and oxidant

inferredcites →https://doi.org/10.1016/s0040-4039(99)01022-9openalex-snapshot

PaaSicats: Powerful catalysts for asymmetric epoxidation of enones. Novel syntheses of α-arylpropanoic acids including (S)-fenoprofen

inferredcites →https://doi.org/10.1016/s0957-4166(00)80284-0openalex-snapshot

NMR measurements and semi-empirical calculations in a first approach to elucidate the mechanism of enantioselective cyanohydrin formation catalysed by cyclo-(S)-Phe-(S)-His

inferredcites →https://doi.org/10.1016/s0957-4166(00)80358-4openalex-snapshot

The oxidation of benzaldehyde to benzoic acid catalysed by cyclo-[(S)-His-(S)-Phe], and its implications for the catalytic asymmetric addition of HCN to aldehydes.

inferredcites →https://doi.org/10.1016/s0957-4166(02)00485-8openalex-snapshot

An exploration of asymmetric Baylis–Hillman reactions catalyzed by quinidine-derived chiral amines

inferredcites →https://doi.org/10.1016/s0957-4166(97)00178-xopenalex-snapshot

Catalytic enantioselective addition of hydrogen cyanide to benzaldehyde and p-methoxybenzaldehyde using cyclo-His-(α-Me)Phe as catalyst

inferredcites →https://doi.org/10.1016/s0957-4166(98)00420-0openalex-snapshot

The use of sonochemistry in the asymmetric epoxidation of substituted chalcones with sodium perborate tetrahydrate

inferredcites →https://doi.org/10.1016/s0959-440x(98)80124-3openalex-snapshot

Functionalization of designed folded polypeptides

inferredcites →https://doi.org/10.1016/s0960-894x(00)00315-2openalex-snapshot

Preparation of l-α-phosphatidyl-d-myo-inositol 3-phosphate (3-PIP) and 3,5-bisphosphate (3,5-PIP2)

inferredcites →https://doi.org/10.1016/s0960-894x(03)00498-0openalex-snapshot

Discovery of new peptide-Based catalysts for the direct asymmetric aldol reaction

inferredcites →https://doi.org/10.1016/s0968-0896(98)00218-1openalex-snapshot

Designed four-helix bundle catalysts—the engineering of reactive sites for hydrolysis and transesterification reactions of p-nitrophenyl esters

inferredcites →https://doi.org/10.1016/s1367-5931(02)00324-1openalex-snapshot

Proton-activated fluorescence as a tool for simultaneous screening of combinatorial chemical reactions

inferredcites →https://doi.org/10.1021/ar0300468openalex-snapshot

Enamine-Based Organocatalysis with Proline and Diamines: The Development of Direct Catalytic Asymmetric Aldol, Mannich, Michael, and Diels−Alder Reactions

inferredcites →https://doi.org/10.1021/ar030051bopenalex-snapshot

Asymmetric Catalysis with “Planar-Chiral” Derivatives of 4-(Dimethylamino)pyridine

inferredcites →https://doi.org/10.1021/ar030061copenalex-snapshot

In Search of Peptide-Based Catalysts for Asymmetric Organic Synthesis

inferredcites →https://doi.org/10.1021/ar050203yopenalex-snapshot

Peptide Dendrimers as Artificial Enzymes, Receptors, and Drug-Delivery Agents

inferredcites →https://doi.org/10.1021/cr020038popenalex-snapshot

Catalytic Enantioselective Strecker Reactions and Analogous Syntheses

inferredcites →https://doi.org/10.1021/cr990372uopenalex-snapshot

Recent Developments in the Synthesis and Utilization of Chiral Sulfoxides

inferredcites →https://doi.org/10.1021/ja00035a053openalex-snapshot

Conformation-controlled hydrolysis of polyribonucleotides by sequential basic polypeptides

inferredcites →https://doi.org/10.1021/ja001460vopenalex-snapshot

Catalytic Asymmetric Synthesis of anti-1,2-Diols

inferredcites →https://doi.org/10.1021/ja00213a035openalex-snapshot

Membrane matrix for the hydrolysis of amino acid esters with marked enantioselectivity

inferredcites →https://doi.org/10.1021/ja00228a045openalex-snapshot

Basic polypeptides accelerate the hydrolysis of ribonucleic acids

inferredcites →https://doi.org/10.1021/ja00248a038openalex-snapshot

Experimental and computer modeling studies of micellar diastereoselectivity

inferredcites →https://doi.org/10.1021/ja00293a067openalex-snapshot

Extraordinary micellar enantioselectivity coupled to altered aggregate structure

inferredcites →https://doi.org/10.1021/ja00321a028openalex-snapshot

Stereochemical studies of the electrolytic reactions of organic compounds. 25. Electroorganic reactions on organic electrodes. 6. Electrochemical asymmetric oxidation of unsymmetric sulfides to the corresponding chiral sulfoxides on poly(amino acid)-coated electrodes

inferredcites →https://doi.org/10.1021/ja00336a034openalex-snapshot

Origins of micellar diastereoselectivity

inferredcites →https://doi.org/10.1021/ja00349a046openalex-snapshot

Stereochemical studies of the electrolytic reactions of organic compounds. 19. Electroorganic reactions on organic electrodes. 1. Asymmetric reduction of prochiral activated olefins on a poly-L-valine-coated graphite

inferredcites →https://doi.org/10.1021/ja00355a029openalex-snapshot

Stereochemical studies of the electrolytic reactions of organic compounds. Part 22. Electroorganic reactions on organic electrodes. 3. Electrochemical asymmetric oxidation of phenyl cyclohexyl sulfide on poly(L-valine)-coated platinum electrodes

inferredcites →https://doi.org/10.1021/ja00393a068openalex-snapshot

Functionalized vesicular assembly. Enantioselective catalysis of ester hydrolysis

inferredcites →https://doi.org/10.1021/ja00411a009openalex-snapshot

Multiconformational synthetic polypeptides

inferredcites →https://doi.org/10.1021/ja00441a070openalex-snapshot

Oxidations on DSA and chirally modified DSA and tin dioxide electrodes

inferredcites →https://doi.org/10.1021/ja00503a051openalex-snapshot

Micellar stereoselectivity. Cleavage of diastereomeric substrates by functional surfactant micelles

inferredcites →https://doi.org/10.1021/ja00541a084openalex-snapshot

Metal clusters with exposed and low-coordinate nitride nitrogen atoms

inferredcites →https://doi.org/10.1021/ja00845a061openalex-snapshot

Chiral electrode

inferredcites →https://doi.org/10.1021/ja0108584openalex-snapshot

Selection of Enantioselective Acyl Transfer Catalysts from a Pooled Peptide Library through a Fluorescence-Based Activity Assay: An Approach to Kinetic Resolution of Secondary Alcohols of Broad Structural Scope

inferredcites →https://doi.org/10.1021/ja01547a064openalex-snapshot

On the Mechanism of Thiamine Action. IV.1 Evidence from Studies on Model Systems

inferredcites →https://doi.org/10.1021/ja0165943openalex-snapshot

Synthesis of α-Amido Ketones via Organic Catalysis: Thiazolium-Catalyzed Cross-Coupling of Aldehydes with Acylimines

inferredcites →https://doi.org/10.1021/ja016779+openalex-snapshot

Discovery of a Catalytic Asymmetric Phosphorylation through Selection of a Minimal Kinase Mimic: A Concise Total Synthesis of d -myo-Inositol-1-Phosphate

inferredcites →https://doi.org/10.1021/ja017774fopenalex-snapshot

Aqueous Aldol Catalysis by a Nicotine Metabolite

inferredcites →https://doi.org/10.1021/ja0177814openalex-snapshot

Asymmetric Azidation−Cycloaddition with Open-Chain Peptide-Based Catalysts. A Sequential Enantioselective Route to Triazoles

inferredcites →https://doi.org/10.1021/ja027402mopenalex-snapshot

Enantiodivergence in Small-Molecule Catalysis of Asymmetric Phosphorylation: Concise Total Syntheses of the Enantiomeric d -myo-Inositol-1-phosphate and d -myo-Inositol-3-phosphate

inferredcites →https://doi.org/10.1021/ja034528qopenalex-snapshot

Novel Small Organic Molecules for a Highly Enantioselective Direct Aldol Reaction

inferredcites →https://doi.org/10.1021/ja042650zopenalex-snapshot

Thiazolylalanine-Derived Catalysts for Enantioselective Intermolecular Aldehyde−Imine Cross-Couplings

inferredcites →https://doi.org/10.1021/ja044652popenalex-snapshot

A Strong Positive Dendritic Effect in a Peptide Dendrimer-Catalyzed Ester Hydrolysis Reaction

inferredcites →https://doi.org/10.1021/ja0466098openalex-snapshot

Asymmetric Syntheses of Phosphatidylinositol-3-Phosphates with Saturated and Unsaturated Side Chains through Catalytic Asymmetric Phosphorylation

inferredcites →https://doi.org/10.1021/ja047360xopenalex-snapshot

Chemistry and Biology of Deoxy-myo-inositol Phosphates: Stereospecificity of Substrate Interactions within an Archaeal and a Bacterial IMPase

inferredcites →https://doi.org/10.1021/ja047845lopenalex-snapshot

Catalytic Enantioselective Synthesis of Sulfinate Esters through the Dynamic Resolution of tert -Butanesulfinyl Chloride

inferredcites →https://doi.org/10.1021/ja0491477openalex-snapshot

2,3-Dihydroimidazo[1,2-a]pyridines: A New Class of Enantioselective Acyl Transfer Catalysts and Their Use in Kinetic Resolution of Alcohols

inferredcites →https://doi.org/10.1021/ja049276nopenalex-snapshot

Selective Catalysis with Peptide Dendrimers

inferredcites →https://doi.org/10.1021/ja049661copenalex-snapshot

Structure-Selectivity Relationships and Structure for a Peptide-Based Enantioselective Acylation Catalyst

inferredcites →https://doi.org/10.1021/ja067840jopenalex-snapshot

Remote Desymmetrization at Near-Nanometer Group Separation Catalyzed by a Miniaturized Enzyme Mimic

inferredcites →https://doi.org/10.1021/ja952686eopenalex-snapshot

Asymmetric Catalysis of the Strecker Amino Acid Synthesis by a Cyclic Dipeptide

inferredcites →https://doi.org/10.1021/ja961097lopenalex-snapshot

The Mechanism of Self-Catalyzed Site-Selective Functionalization of a Designed Helix−Loop−Helix Motif

inferredcites →https://doi.org/10.1021/ja970854sopenalex-snapshot

Catalysis of Hydrolysis and Transesterification Reactions of p-Nitrophenyl Esters by a Designed Helix−Loop−Helix Dimer

inferredcites →https://doi.org/10.1021/ja9737580openalex-snapshot

Cooperative Nucleophilic and General-Acid Catalysis by the HisH+−His Pair and Arginine Transition State Binding in Catalysis of Ester Hydrolysis Reactions by Designed Helix−Loop−Helix Motifs

inferredcites →https://doi.org/10.1021/ja973892kopenalex-snapshot

Kinetic Resolution of Alcohols Catalyzed by Tripeptides Containing the N-Alkylimidazole Substructure

inferredcites →https://doi.org/10.1021/ja980682eopenalex-snapshot

Substrate Recognition and Saturation Kinetics in de Novo Designed Histidine-Based Four-Helix Bundle Catalysts

inferredcites →https://doi.org/10.1021/ja992655+openalex-snapshot

Chiral Amine-Catalyzed Asymmetric Baylis−Hillman Reaction: A Reliable Route to Highly Enantiomerically Enriched (α-Methylene-β-hydroxy)esters

inferredcites →https://doi.org/10.1021/ja9931776openalex-snapshot

A Biomimetic Approach to Asymmetric Acyl Transfer Catalysis

inferredcites →https://doi.org/10.1021/ja994280yopenalex-snapshot

Proline-Catalyzed Direct Asymmetric Aldol Reactions

inferredcites →https://doi.org/10.1021/jo00012a019openalex-snapshot

Mechanism of enantioselective ester cleavage by histidine containing dipeptides at a micellar interface

inferredcites →https://doi.org/10.1021/jo00075a019openalex-snapshot

A practical, enantioselective synthesis of SK&F 104353

inferredcites →https://doi.org/10.1021/jo00116a016openalex-snapshot

Hybrid Liposomes Coupled to Steric Control with High Enantioselectivity

inferredcites →https://doi.org/10.1021/jo00194a019openalex-snapshot

Effect of cholesterol on the stereoselective hydrolysis in artificial membrane systems

inferredcites →https://doi.org/10.1021/jo00248a046openalex-snapshot

Lipase-catalyzed irreversible transesterification for preparative synthesis of chiral glycerol derivatives

inferredcites →https://doi.org/10.1021/jo00256a065openalex-snapshot

Synthetic studies of the nargenicins. Introduction of the C14-C19 side chain by diastereoselective [2,3] Wittig rearrangement of a tertiary allylic ether

inferredcites →https://doi.org/10.1021/jo00288a030openalex-snapshot

The cyclic dipeptide cyclo[(S)-phenylalanyl-(S)-histidyl] as a catalyst for asymmetric addition of hydrogen cyanide to aldehydes

inferredcites →https://doi.org/10.1021/jo00309a027openalex-snapshot

Studies on thermodynamics for hydrolysis. 3. Isokinetic temperature related to molecular location of reactants in coaggregates

inferredcites →https://doi.org/10.1021/jo00311a024openalex-snapshot

Polymer-supported poly(amino acids) as new asymmetric epoxidation catalyst of .alpha.,.beta.-unsaturated ketones

inferredcites →https://doi.org/10.1021/jo00890a018openalex-snapshot

Generation and synthetic applications of 2-lithio-1,3-dithianes

inferredcites →https://doi.org/10.1021/jo00922a015openalex-snapshot

Micellar catalysis of ester hydrolysis. Influence of chirality and head group structure in simple surfactants

inferredcites →https://doi.org/10.1021/jo015803zopenalex-snapshot

Fluorescence-Based Screening of Asymmetric Acylation Catalysts through Parallel Enantiomer Analysis. Identification of a Catalyst for Tertiary Alcohol Resolution

inferredcites →https://doi.org/10.1021/jo0269013openalex-snapshot

Enantioselective Synthesis of an Aziridinomitosane and Selective Functionalizations of a Key Intermediate

inferredcites →https://doi.org/10.1021/jo030007+openalex-snapshot

A Comparison of Monocyclic and Bicyclic Phospholanes as Acyl-Transfer Catalysts

inferredcites →https://doi.org/10.1021/jo030279copenalex-snapshot

Desymmetrization of meso-Hydrobenzoin Using Chiral, Nucleophilic Phosphine Catalysts

inferredcites →https://doi.org/10.1021/jo040107vopenalex-snapshot

Role of Secondary Structure in the Asymmetric Acylation Reaction Catalyzed by Peptides Based on Chiral Cα-Tetrasubstituted α-Amino Acids

inferredcites →https://doi.org/10.1021/jo050202jopenalex-snapshot

A New Interpretation of the Baylis−Hillman Mechanism

inferredcites →https://doi.org/10.1021/jo050257lopenalex-snapshot

Dipeptide-Catalyzed Asymmetric Aldol Condensation of Acetone with (N-Alkylated) Isatins

inferredcites →https://doi.org/10.1021/jo060273yopenalex-snapshot

Synthesis and Activity of Histidine-Containing Catalytic Peptide Dendrimers

inferredcites →https://doi.org/10.1021/jo060702sopenalex-snapshot

Streamlined Synthesis of Phosphatidylinositol (PI), PI3P, PI3,5P2, and Deoxygenated Analogues as Potential Biological Probes

inferredcites →https://doi.org/10.1021/jo0610816openalex-snapshot

Unified Total Syntheses of the Inositol Polyphosphates: d -I-3,5,6P3, d -I-3,4,5P3, d -I-3,4,6P3, and d -I-3,4,5,6P4 via Catalytic Enantioselective and Site-Selective Phosphorylation

inferredcites →https://doi.org/10.1021/jo960602uopenalex-snapshot

Synthesis of the D-3 Series of Phosphatidylinositol Phosphates

inferredcites →https://doi.org/10.1021/jo980501ropenalex-snapshot

Asymmetric Total Synthesis of Phosphatidylinositol 3-Phosphate and 4-Phosphate Derivatives

inferredcites →https://doi.org/10.1021/jo981642wopenalex-snapshot

Minimal Acylase-Like Peptides. Conformational Control of Absolute Stereospecificity

inferredcites →https://doi.org/10.1021/ol000170gopenalex-snapshot

Catalytic Asymmetric Conjugate Addition of Nitroalkanes to Cycloalkenones

inferredcites →https://doi.org/10.1021/ol007005lopenalex-snapshot

Efficient Asymmetric Epoxidation of α,β-Unsaturated Ketones Using a Soluble Triblock Polyethylene Glycol−Polyamino Acid Catalyst

inferredcites →https://doi.org/10.1021/ol016372+openalex-snapshot

Enantioselective Synthesis of a Mitosane Core Assisted by Diversity-Based Catalyst Discovery

inferredcites →https://doi.org/10.1021/ol0166451openalex-snapshot

Highly Enantioselective Enone Epoxidation Catalyzed by Short Solid Phase-Bound Peptides: Dominant Role of Peptide Helicity

inferredcites →https://doi.org/10.1021/ol035466bopenalex-snapshot

Dual Catalyst Control in the Amino Acid-Peptide-Catalyzed Enantioselective Baylis−Hillman Reaction

inferredcites →https://doi.org/10.1021/ol049141mopenalex-snapshot

Small Peptides Catalyze Highly Enantioselective Direct Aldol Reactions of Aldehydes with Hydroxyacetone: Unprecedented Regiocontrol in Aqueous Media

inferredcites →https://doi.org/10.1021/ol0500259openalex-snapshot

Increased Structural Complexity Leads to Higher Activity: Peptides as Efficient and Versatile Catalysts for Asymmetric Aldol Reactions

inferredcites →https://doi.org/10.1021/ol050275popenalex-snapshot

Catalytic Enantioselective Sulfinyl Transfer Using Cinchona Alkaloid Catalysts

inferredcites →https://doi.org/10.1021/ol051061aopenalex-snapshot

Desymmetrization of Glycerol Derivatives with Peptide-Based Acylation Catalysts

inferredcites →https://doi.org/10.1021/ol051063vopenalex-snapshot

Kinetic Resolution of Alcohols Using a 1,2-Dihydroimidazo[1,2-a]quinoline Enantioselective Acylation Catalyst

inferredcites →https://doi.org/10.1021/ol051708ropenalex-snapshot

Mechanistic Insights from Reaction Progress Kinetic Analysis of the Polypeptide-Catalyzed Epoxidation of Chalcone

inferredcites →https://doi.org/10.1021/ol0603007openalex-snapshot

Catalytic Asymmetric Protonation of Lithium Enolates Using Amino Acid Derivatives as Chiral Proton Sources

inferredcites →https://doi.org/10.1021/ol9909076openalex-snapshot

Amine-Catalyzed Addition of Azide Ion to α,β-Unsaturated Carbonyl Compounds

inferredcites →https://doi.org/10.1021/op0300037openalex-snapshot

Development of the Juliá−Colonna Asymmetric Epoxidation Reaction: Part 1. Preparation and Activation of the Polyleucine Catalyst

inferredcites →https://doi.org/10.1039/a605776dopenalex-snapshot

Site selectivity in self-catalysed functionalization of helical polypeptide structures

inferredcites →https://doi.org/10.1039/a605908bopenalex-snapshot

The relationship between structure and reactivity in RA-42, a designed helix–loop–helix motif

inferredcites →https://doi.org/10.1039/a700550dopenalex-snapshot

Asymmetric epoxidation of enones employing polymeric α-amino acids in non-aqueous media

inferredcites →https://doi.org/10.1039/a703214eopenalex-snapshot

The site-selective incorporation of a NAD + cofactor mimic into a folded helix–loop–helix polypeptide motif

inferredcites →https://doi.org/10.1039/a704413eopenalex-snapshot

Improved procedure for Juliá–Colonna asymmetric epoxidation of α,β-unsaturated ketones: total synthesis of diltiazem and Taxol TM side-chain

showing the first 200 of 274 · page through all 274

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4666632openalex-extracted

Exploring Green Solvents and Solvent-Free Conditions for Sustainable Organocatalysis

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Chiral Compounds

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Assembly‐driven protection from hydrolysis as key selective force during chemical evolution

inferred← citeshttps://doi.org/10.1002/9780470661345.smc156openalex-snapshot

Supramolecular Organocatalysis

inferred← citeshttps://doi.org/10.1002/9781118063965.ch4openalex-snapshot

Peptide‐Catalyzed Asymmetric Synthesis

inferred← citeshttps://doi.org/10.1002/9781118087992.ch13openalex-snapshot

Peptides for Asymmetric Catalysis

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Organozymes: Molecular Engineering and Combinatorial Selection of Peptidic Organo‐ and Transition‐Metal Catalysts

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Monoterpenes and Iridoids

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ASYMMETRIC PEPTIDE CATALYSIS

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(Thio)urea Organocatalysts

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Organocatalysis

inferred← citeshttps://doi.org/10.1002/9783527628698.hgc081openalex-snapshot

Synthesis Without Metals

inferred← citeshttps://doi.org/10.1002/9783527631780.ch10openalex-snapshot

Catalysis by Peptide‐Based Enzyme Models

inferred← citeshttps://doi.org/10.1002/9783527650880.ch3openalex-snapshot

Catalytic Kinetic Resolution

inferred← citeshttps://doi.org/10.1002/9783527658862.ch10openalex-snapshot

Brønsted Acids

inferred← citeshttps://doi.org/10.1002/9783527658862.ch37openalex-snapshot

Formation of 3‐, 4‐ and 5‐Membered Cycles by Intermolecular Reactions

inferred← citeshttps://doi.org/10.1002/9783527658862.ch41openalex-snapshot

Regio‐ and Position Selective Reactions and Desymmetrizations

inferred← citeshttps://doi.org/10.1002/9783527658862.ch5openalex-snapshot

Oligopeptides as Modular Organocatalytic Scaffolds

inferred← citeshttps://doi.org/10.1002/9783527675142.ch12openalex-snapshot

Chiral Lewis Base Activation of Acyl and Related Donors in Enantioselective Transformations ( n ?→?π * )

inferred← citeshttps://doi.org/10.1002/9783527681020.ch10openalex-snapshot

Catalysis by Artificial Oligopeptides

inferred← citeshttps://doi.org/10.1002/9783527802029.ch3openalex-snapshot

Asymmetric Epoxidation

inferred← citeshttps://doi.org/10.1002/9783527809080.cataz12574openalex-snapshot

peptides

inferred← citeshttps://doi.org/10.1002/9783527832033.ch6openalex-snapshot

Catalytic Supramolecular Gels

inferred← citeshttps://doi.org/10.1002/9783527832217.ch21openalex-snapshot

Mayr Linear Free Energy Relationship: A Powerful Tool for Understanding Aminocatalyzed Reactions

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Investigating Sequence Space: How Important is the Spatial Arrangement of Functional Groups in the Asymmetric Aldol Reaction Catalyst H‐Pro‐Pro‐Asp‐NH2?

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Asymmetric Epoxidation of α,β‐Unsaturated Aldehydes in Aqueous Media Catalyzed by Resin‐Supported Peptide‐ Containing Unnatural Amino Acids

inferred← citeshttps://doi.org/10.1002/adsc.201100111openalex-snapshot

Catalytic Non‐Enzymatic Kinetic Resolution

inferred← citeshttps://doi.org/10.1002/adsc.201100118openalex-snapshot

Efficient Recovery and Reuse of an Immobilized Peptidic Organocatalyst

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Highly Enantioselective Co‐Catalytic Direct Aldol Reactions by Combination of Hydrogen‐Bond Donating and Acyclic Amino Acid Catalysts

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The Growing Impact of Catalysis in the Pharmaceutical Industry

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Effect of the Helical Tether of a Resin‐Supported Peptide Catalyst for Friedel–Crafts‐Type Alkylation in Water

inferred← citeshttps://doi.org/10.1002/adsc.201200611openalex-snapshot

Asymmetric α‐Amination of Aldehydes by a Recyclable Resin‐Supported Peptide Catalyst

inferred← citeshttps://doi.org/10.1002/adsc.201400415openalex-snapshot

Chiral Bicyclic Imidazole Nucleophilic Catalysts: Design, Synthesis, and Application to the Kinetic Resolution of Arylalkylcarbinols

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Enantioselective Titanium‐Catalyzed Cyanation Reactions of Carbonyl Compounds

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2,6‐Bis(amido)benzoic Acid with Internal Hydrogen Bond as Brønsted Acid Catalyst for Friedel–Crafts Reaction of Indoles

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Heterogeneous Dipeptide‐Catalyzed α‐Amination of Aldehydes in a Continuous‐Flow Reactor: Effect of Residence Time on Enantioselectivity

inferred← citeshttps://doi.org/10.1002/adsc.201500557openalex-snapshot

Dearomatization of Indoles via a Phenol‐Directed Vanadium‐ Catalyzed Asymmetric Epoxidation and Ring‐Opening Cascade

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Novel Easily Recyclable Bifunctional Phosphonic Acid Carrying Tripeptides for the Stereoselective Michael Addition of Aldehydes with Nitroalkenes

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Catalytic Asymmetric Allylation of 3‐Aryloxindoles by Merging Palladium Catalysis and Asymmetric H‐Bonding Catalysis

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Tetrahydropyran‐Based Hybrid Dipeptides as Asymmetric Catalysts for Michael Addition of Aldehydes to β‐Nitrostyrenes

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Phosphonium Salts in Asymmetric Catalysis: A Journey in a Decade's Extensive Research Work

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Iodine‐Catalyzed Oxidative Rearrangement of Amines to α‐Amino Acetals and α‐Amino Aldehydes

inferred← citeshttps://doi.org/10.1002/adsc.201900247openalex-snapshot

Conformational Control of Tetrahydropyran‐Based Hybrid Dipeptide Catalysts Improves Activity and Stereoselectivity

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Recent Developments in Enantioselective Multicatalyzed Tandem Reactions

inferred← citeshttps://doi.org/10.1002/adsc.202000753openalex-snapshot

Advances in Asymmetric Amino Acid Synthesis Enabled by Radical Chemistry

inferred← citeshttps://doi.org/10.1002/adsc.202100313openalex-snapshot

Organocatalytic Enantioselective Friedel‐Crafts Alkylation Reactions of Pyrroles

inferred← citeshttps://doi.org/10.1002/adsc.70156openalex-snapshot

Revisiting the Role of Intramolecular Proton Donation in ATC Foldamer Catalysts for Asymmetric Nitro‐Michael Reactions

inferred← citeshttps://doi.org/10.1002/adsc.70819openalex-snapshot

Advances in Transition‐Metal‐Catalyzed 1,2‐N‐Migrations via Carbon‐Centered Carbenes and Radicals

inferred← citeshttps://doi.org/10.1002/ajoc.201400028openalex-snapshot

Development of a Peptide‐Based Primary Aminocatalyst with a Helical Structure

inferred← citeshttps://doi.org/10.1002/ajoc.201402040openalex-snapshot

Design of Peptidyl Thiourea Derivatives as Organocatalysts for the Asymmetric Ring Opening of meso ‐Stilbene Oxides

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Synthesis and Evaluation of (S)‐Proline‐Containing α,β‐Dipeptides as Organocatalysts in Solvent‐Free Asymmetric Aldol Reactions Under Ball‐Milling Conditions

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Ru–Prolinamide‐Catalyzed Asymmetric Transfer Hydrogenation of Racemic β‐Heterosubstituted Cycloalkanones Driven by Dynamic Kinetic Resolution

inferred← citeshttps://doi.org/10.1002/ajoc.202300113openalex-snapshot

Design of Threonine‐Derived Amino Sulfonamide Organocatalysts for the Highly Stereoselective Aldol Reactions

inferred← citeshttps://doi.org/10.1002/ange.200800641openalex-snapshot

Enantioselektive kinetische Racematspaltung von trans‐Cycloalkan‐1,2‐diolen

inferred← citeshttps://doi.org/10.1002/ange.200801366openalex-snapshot

Helical Peptide Arrays on Self‐Assembled Monolayer Surfaces through Soft and Reactive Landing of Mass‐Selected Ions

inferred← citeshttps://doi.org/10.1002/ange.200803583openalex-snapshot

“Covalent Capture”: Verschmelzung von kovalenter und nichtkovalenter Synthese

inferred← citeshttps://doi.org/10.1002/ange.201002127openalex-snapshot

An Efficient Titanium Catalyst for Enantioselective Cyanation of Aldehydes: Cooperative Catalysis

inferred← citeshttps://doi.org/10.1002/ange.201003014openalex-snapshot

Ein zweikerniger Titankatalysator zur enantioselektiven Cyanierung von Aldehyden durch kooperative Katalyse

inferred← citeshttps://doi.org/10.1002/ange.201003646openalex-snapshot

Copper‐Catalyzed Rearrangement of Tertiary Amines through Oxidation of Aliphatic CH Bonds in Air or Oxygen: Direct Synthesis of α‐Amino Acetals

inferred← citeshttps://doi.org/10.1002/ange.201005109openalex-snapshot

Solvent‐Dependent Enantiodivergent Mannich‐Type Reaction: Utilizing a Conformationally Flexible Guanidine/Bisthiourea Organocatalyst

inferred← citeshttps://doi.org/10.1002/ange.201006128openalex-snapshot

Organokatalytischer, enantioselektiver Acyltransfer auf racemische sowie meso‐Alkohole, ‐Amine und ‐Thiole

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The Direct Asymmetric Vinylogous Aldol Reaction of Furanones with α‐Ketoesters: Access to Chiral γ‐Butenolides and Glycerol Derivatives

inferred← citeshttps://doi.org/10.1002/ange.201008031openalex-snapshot

Atropselektive Organokatalyse

inferred← citeshttps://doi.org/10.1002/ange.201100918openalex-snapshot

Direkte katalytische asymmetrische Reaktionen unter Protonentransferkatalyse

inferred← citeshttps://doi.org/10.1002/ange.201102094openalex-snapshot

Highly Enantioselective [3+2] Annulation of Morita–Baylis–Hillman Adducts Mediated by L ‐Threonine‐Derived Phosphines: Synthesis of 3‐Spirocyclopentene‐2‐oxindoles having Two Contiguous Quaternary Centers

inferred← citeshttps://doi.org/10.1002/ange.201105812openalex-snapshot

Enantioselective Stetter Reactions of Enals and Modified Chalcones Catalyzed by N‐Heterocyclic Carbenes

inferred← citeshttps://doi.org/10.1002/ange.201202512openalex-snapshot

Screening Rhodium Metallopeptide Libraries “On Bead”: Asymmetric Cyclopropanation and a Solution to the Enantiomer Problem

inferred← citeshttps://doi.org/10.1002/ange.201204215openalex-snapshot

α‐Amination of Aldehydes Catalyzed by In Situ Generated Hypoiodite

inferred← citeshttps://doi.org/10.1002/ange.201206373openalex-snapshot

Nanopartikel und Peptide: eine vielversprechende Liaison für die biomimetische Katalyse

inferred← citeshttps://doi.org/10.1002/ange.201206582openalex-snapshot

Asymmetrische Katalyse mit Bis(hydroxyphenyl)diamid/Seltenerdmetall‐Komplexen

inferred← citeshttps://doi.org/10.1002/ange.201206916openalex-snapshot

Construction of an All‐Carbon Quaternary Stereocenter by the Peptide‐Catalyzed Asymmetric Michael Addition of Nitromethane to β‐Disubstituted α,β‐Unsaturated Aldehydes

inferred← citeshttps://doi.org/10.1002/ange.201208285openalex-snapshot

Chiral Phosphine Catalyzed Asymmetric Michael Addition of Oxindoles

inferred← citeshttps://doi.org/10.1002/ange.201305004openalex-snapshot

Peptide‐Catalyzed Regio‐ and Enantioselective Reduction of α,β,γ,δ‐Unsaturated Aldehydes

inferred← citeshttps://doi.org/10.1002/ange.201305644openalex-snapshot

Catalytic Enantioselective Synthesis of Tertiary Thiols From 5H‐Thiazol‐4‐ones and Nitroolefins: Bifunctional Ureidopeptide‐Based Brønsted Base Catalysis

inferred← citeshttps://doi.org/10.1002/ange.201400241openalex-snapshot

Organokatalytische asymmetrische Epoxidierungen – Reaktionen, Mechanismen und Anwendungen

inferred← citeshttps://doi.org/10.1002/ange.201403829openalex-snapshot

Conformationally Constrained Cyclic Peptides: Powerful Scaffolds for Asymmetric Catalysis

inferred← citeshttps://doi.org/10.1002/ange.201409004openalex-snapshot

Dekonstruktion kovalenter Organokatalyse

inferred← citeshttps://doi.org/10.1002/ange.201410268openalex-snapshot

Histidine‐Containing Peptide Catalysts Developed by a Facile Library Screening Method

inferred← citeshttps://doi.org/10.1002/ange.201505898openalex-snapshot

Phosphothreonine as a Catalytic Residue in Peptide‐Mediated Asymmetric Transfer Hydrogenations of 8‐Aminoquinolines

inferred← citeshttps://doi.org/10.1002/ange.201509863openalex-snapshot

The Enantioselective Dakin–West Reaction

inferred← citeshttps://doi.org/10.1002/ange.201602230openalex-snapshot

Peptide‐Catalyzed Stereoselective Conjugate Addition Reactions of Aldehydes to Maleimide

inferred← citeshttps://doi.org/10.1002/ange.201602751openalex-snapshot

Allosterically Regulated Phosphatase Activity from Peptide–PNA Conjugates Folded Through Hybridization

inferred← citeshttps://doi.org/10.1002/ange.201605754openalex-snapshot

Synthesis of Aminoboronic Acid Derivatives from Amines and Amphoteric Boryl Carbonyl Compounds

inferred← citeshttps://doi.org/10.1002/ange.201608559openalex-snapshot

Aufklärung entscheidender struktureller Aspekte einer enantioselektiven Peptid‐katalysierten Acylierung mittels moderner NMR‐Techniken

inferred← citeshttps://doi.org/10.1002/ange.201609631openalex-snapshot

Bioorthogonal Diversification of Peptides through Selective Ruthenium(II)‐Catalyzed C–H Activation

inferred← citeshttps://doi.org/10.1002/ange.201610693openalex-snapshot

Synthesis of Chiral Vicinal Diamines by Silver(I)‐Catalyzed Enantioselective Aminolysis of N‐Tosylaziridines

inferred← citeshttps://doi.org/10.1002/ange.201811668openalex-snapshot

Late‐Stage Peptide Diversification through Cobalt‐Catalyzed C−H Activation: Sequential Multicatalysis for Stapled Peptides

inferred← citeshttps://doi.org/10.1002/ange.201812705openalex-snapshot

Late‐Stage Diversification through Manganese‐Catalyzed C−H Activation: Access to Acyclic, Hybrid, and Stapled Peptides

inferred← citeshttps://doi.org/10.1002/ange.201812864openalex-snapshot

Chiral DMAP‐N‐oxides as Acyl Transfer Catalysts: Design, Synthesis, and Application in Asymmetric Steglich Rearrangement

inferred← citeshttps://doi.org/10.1002/ange.201913563openalex-snapshot

Peptide‐Catalyzed Fragment Couplings that Form Axially Chiral Non‐C2‐Symmetric Biaryls

inferred← citeshttps://doi.org/10.1002/ange.202008369openalex-snapshot

Carbene‐Catalyzed Enantioselective Aldol Reaction: Post‐Aldol Stereochemistry Control and Formation of Quaternary Stereogenic Centers

inferred← citeshttps://doi.org/10.1002/ange.202012909openalex-snapshot

Visible‐Light‐Enabled Enantioconvergent Synthesis of α‐Amino Acid Derivatives via Synergistic Brønsted Acid/Photoredox Catalysis

inferred← citeshttps://doi.org/10.1002/ange.202109694openalex-snapshot

Tunable and Cooperative Catalysis for Enantioselective Pictet‐Spengler Reaction with Varied Nitrogen‐Containing Heterocyclic Carboxaldehydes

inferred← citeshttps://doi.org/10.1002/ange.202114129openalex-snapshot

Chiral 1,2,3‐Triazolium Salt Catalyzed Asymmetric Mono‐ and Dialkylation of 2,5‐Diketopiperazines with the Construction of Tetrasubstituted Carbon Centers

inferred← citeshttps://doi.org/10.1002/ange.202201788openalex-snapshot

Catalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoamides Catalyzed by a Single H‐Bond Donor Organocatalyst

inferred← citeshttps://doi.org/10.1002/ange.202202552openalex-snapshot

Highly Enantioselective Synthesis of N‐Unprotected Unnatural α‐Amino Acid Derivatives by Ruthenium‐Catalyzed Direct Asymmetric Reductive Amination

inferred← citeshttps://doi.org/10.1002/ange.202300537openalex-snapshot

Organocatalytic Synthesis of Triflones Bearing Two Non‐Adjacent Stereogenic Centers

inferred← citeshttps://doi.org/10.1002/ange.202307258openalex-snapshot

Design and Application of Peptide‐Mimic Phosphonium Salt Catalysts in Asymmetric Synthesis

inferred← citeshttps://doi.org/10.1002/ange.202310112openalex-snapshot

Combinatorial Ligand Assisted Simultaneous Control of Axial and Central Chirality in Highly Stereoselective C−H Allylation

inferred← citeshttps://doi.org/10.1002/ange.202316364openalex-snapshot

Advances and Prospects in Understanding London Dispersion Interactions in Molecular Chemistry

inferred← citeshttps://doi.org/10.1002/ange.202421062openalex-snapshot

Investigating Interaction Dynamics of an Enantioselective Peptide‐Catalyzed Acylation Reaction

inferred← citeshttps://doi.org/10.1002/ange.202516385openalex-snapshot

Stereoselective Synthesis of Cyclic P(V) Compounds via Stereoconvergent Nucleophilic Substitution

inferred← citeshttps://doi.org/10.1002/ange.5562213openalex-snapshot

Synergistic Ion‐Pair/Lewis Acid Catalysis Enables Enantioselective Synthesis of Helically Chiral Oxa[6]Helicenes

inferred← citeshttps://doi.org/10.1002/anie.200800641openalex-snapshot

Enantioselective Kinetic Resolution of trans‐Cycloalkane‐1,2‐diols

inferred← citeshttps://doi.org/10.1002/anie.200801366openalex-snapshot

Helical Peptide Arrays on Self‐Assembled Monolayer Surfaces through Soft and Reactive Landing of Mass‐Selected Ions

inferred← citeshttps://doi.org/10.1002/anie.200803583openalex-snapshot

Covalent Capture: Merging Covalent and Noncovalent Synthesis

inferred← citeshttps://doi.org/10.1002/anie.201002127openalex-snapshot

An Efficient Titanium Catalyst for Enantioselective Cyanation of Aldehydes: Cooperative Catalysis

inferred← citeshttps://doi.org/10.1002/anie.201003014openalex-snapshot

A Bimetallic Titanium Catalyst for the Enantioselective Cyanation of Aldehydes Based on Cooperative Catalysis

inferred← citeshttps://doi.org/10.1002/anie.201003646openalex-snapshot

Copper‐Catalyzed Rearrangement of Tertiary Amines through Oxidation of Aliphatic CH Bonds in Air or Oxygen: Direct Synthesis of α‐Amino Acetals

inferred← citeshttps://doi.org/10.1002/anie.201005109openalex-snapshot

Solvent‐Dependent Enantiodivergent Mannich‐Type Reaction: Utilizing a Conformationally Flexible Guanidine/Bisthiourea Organocatalyst

inferred← citeshttps://doi.org/10.1002/anie.201006128openalex-snapshot

Organocatalytic Enantioselective Acyl Transfer onto Racemic as well as meso Alcohols, Amines, and Thiols

inferred← citeshttps://doi.org/10.1002/anie.201006316openalex-snapshot

The Direct Asymmetric Vinylogous Aldol Reaction of Furanones with α‐Ketoesters: Access to Chiral γ‐Butenolides and Glycerol Derivatives

inferred← citeshttps://doi.org/10.1002/anie.201008031openalex-snapshot

Atroposelective Organocatalysis

inferred← citeshttps://doi.org/10.1002/anie.201100918openalex-snapshot

Recent Advances in Direct Catalytic Asymmetric Transformations under Proton‐Transfer Conditions

inferred← citeshttps://doi.org/10.1002/anie.201102094openalex-snapshot

inferred← citeshttps://doi.org/10.1002/anie.201105812openalex-snapshot

Enantioselective Stetter Reactions of Enals and Modified Chalcones Catalyzed by N‐Heterocyclic Carbenes

inferred← citeshttps://doi.org/10.1002/anie.201202512openalex-snapshot

Screening Rhodium Metallopeptide Libraries “On Bead”: Asymmetric Cyclopropanation and a Solution to the Enantiomer Problem

inferred← citeshttps://doi.org/10.1002/anie.201204215openalex-snapshot

α‐Amination of Aldehydes Catalyzed by In Situ Generated Hypoiodite

inferred← citeshttps://doi.org/10.1002/anie.201206373openalex-snapshot

Nanoparticles and Peptides: A Fruitful Liaison for Biomimetic Catalysis

inferred← citeshttps://doi.org/10.1002/anie.201206582openalex-snapshot

Asymmetric Catalysis with Bis(hydroxyphenyl)diamides/Rare‐Earth Metal Complexes

inferred← citeshttps://doi.org/10.1002/anie.201206916openalex-snapshot

Construction of an All‐Carbon Quaternary Stereocenter by the Peptide‐Catalyzed Asymmetric Michael Addition of Nitromethane to β‐Disubstituted α,β‐Unsaturated Aldehydes

inferred← citeshttps://doi.org/10.1002/anie.201208285openalex-snapshot

Chiral Phosphine Catalyzed Asymmetric Michael Addition of Oxindoles

inferred← citeshttps://doi.org/10.1002/anie.201305004openalex-snapshot

Peptide‐Catalyzed Regio‐ and Enantioselective Reduction of α,β,γ,δ‐Unsaturated Aldehydes

inferred← citeshttps://doi.org/10.1002/anie.201305644openalex-snapshot

Catalytic Enantioselective Synthesis of Tertiary Thiols From 5H‐Thiazol‐4‐ones and Nitroolefins: Bifunctional Ureidopeptide‐Based Brønsted Base Catalysis

inferred← citeshttps://doi.org/10.1002/anie.201400241openalex-snapshot

Asymmetric Organocatalytic Epoxidations: Reactions, Scope, Mechanisms, and Applications

inferred← citeshttps://doi.org/10.1002/anie.201403829openalex-snapshot

Conformationally Constrained Cyclic Peptides: Powerful Scaffolds for Asymmetric Catalysis

inferred← citeshttps://doi.org/10.1002/anie.201409004openalex-snapshot

Deconstructing Covalent Organocatalysis

inferred← citeshttps://doi.org/10.1002/anie.201410268openalex-snapshot

Histidine‐Containing Peptide Catalysts Developed by a Facile Library Screening Method

inferred← citeshttps://doi.org/10.1002/anie.201505898openalex-snapshot

Phosphothreonine as a Catalytic Residue in Peptide‐Mediated Asymmetric Transfer Hydrogenations of 8‐Aminoquinolines

inferred← citeshttps://doi.org/10.1002/anie.201509863openalex-snapshot

The Enantioselective Dakin–West Reaction

inferred← citeshttps://doi.org/10.1002/anie.201602230openalex-snapshot

Peptide‐Catalyzed Stereoselective Conjugate Addition Reactions of Aldehydes to Maleimide

inferred← citeshttps://doi.org/10.1002/anie.201602751openalex-snapshot

Allosterically Regulated Phosphatase Activity from Peptide–PNA Conjugates Folded Through Hybridization

inferred← citeshttps://doi.org/10.1002/anie.201605754openalex-snapshot

Synthesis of Aminoboronic Acid Derivatives from Amines and Amphoteric Boryl Carbonyl Compounds

inferred← citeshttps://doi.org/10.1002/anie.201608559openalex-snapshot

Uncovering Key Structural Features of an Enantioselective Peptide‐Catalyzed Acylation Utilizing Advanced NMR Techniques

inferred← citeshttps://doi.org/10.1002/anie.201609631openalex-snapshot

Bioorthogonal Diversification of Peptides through Selective Ruthenium(II)‐Catalyzed C–H Activation

inferred← citeshttps://doi.org/10.1002/anie.201610693openalex-snapshot

Synthesis of Chiral Vicinal Diamines by Silver(I)‐Catalyzed Enantioselective Aminolysis of N‐Tosylaziridines

inferred← citeshttps://doi.org/10.1002/anie.201811668openalex-snapshot

Late‐Stage Peptide Diversification through Cobalt‐Catalyzed C−H Activation: Sequential Multicatalysis for Stapled Peptides

inferred← citeshttps://doi.org/10.1002/anie.201812705openalex-snapshot

Late‐Stage Diversification through Manganese‐Catalyzed C−H Activation: Access to Acyclic, Hybrid, and Stapled Peptides

inferred← citeshttps://doi.org/10.1002/anie.201812864openalex-snapshot

Chiral DMAP‐N‐oxides as Acyl Transfer Catalysts: Design, Synthesis, and Application in Asymmetric Steglich Rearrangement

inferred← citeshttps://doi.org/10.1002/anie.201913563openalex-snapshot

Peptide‐Catalyzed Fragment Couplings that Form Axially Chiral Non‐ C 2 ‐Symmetric Biaryls

inferred← citeshttps://doi.org/10.1002/anie.202008369openalex-snapshot

Carbene‐Catalyzed Enantioselective Aldol Reaction: Post‐Aldol Stereochemistry Control and Formation of Quaternary Stereogenic Centers

inferred← citeshttps://doi.org/10.1002/anie.202012909openalex-snapshot

Visible‐Light‐Enabled Enantioconvergent Synthesis of α‐Amino Acid Derivatives via Synergistic Brønsted Acid/Photoredox Catalysis

inferred← citeshttps://doi.org/10.1002/anie.202109694openalex-snapshot

Tunable and Cooperative Catalysis for Enantioselective Pictet‐Spengler Reaction with Varied Nitrogen‐Containing Heterocyclic Carboxaldehydes

inferred← citeshttps://doi.org/10.1002/anie.202114129openalex-snapshot

Chiral 1,2,3‐Triazolium Salt Catalyzed Asymmetric Mono‐ and Dialkylation of 2,5‐Diketopiperazines with the Construction of Tetrasubstituted Carbon Centers

inferred← citeshttps://doi.org/10.1002/anie.202201788openalex-snapshot

Catalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoamides Catalyzed by a Single H‐Bond Donor Organocatalyst

inferred← citeshttps://doi.org/10.1002/anie.202202552openalex-snapshot

Highly Enantioselective Synthesis of N‐Unprotected Unnatural α‐Amino Acid Derivatives by Ruthenium‐Catalyzed Direct Asymmetric Reductive Amination

inferred← citeshttps://doi.org/10.1002/anie.202300537openalex-snapshot

Organocatalytic Synthesis of Triflones Bearing Two Non‐Adjacent Stereogenic Centers

inferred← citeshttps://doi.org/10.1002/anie.202307258openalex-snapshot

Design and Application of Peptide‐Mimic Phosphonium Salt Catalysts in Asymmetric Synthesis

inferred← citeshttps://doi.org/10.1002/anie.202310112openalex-snapshot

Combinatorial Ligand Assisted Simultaneous Control of Axial and Central Chirality in Highly Stereoselective C−H Allylation

inferred← citeshttps://doi.org/10.1002/anie.202316364openalex-snapshot

Advances and Prospects in Understanding London Dispersion Interactions in Molecular Chemistry

inferred← citeshttps://doi.org/10.1002/anie.202421062openalex-snapshot

Investigating Interaction Dynamics of an Enantioselective Peptide‐Catalyzed Acylation Reaction

inferred← citeshttps://doi.org/10.1002/anie.202516385openalex-snapshot

Stereoselective Synthesis of Cyclic P(V) Compounds via Stereoconvergent Nucleophilic Substitution

inferred← citeshttps://doi.org/10.1002/anie.5562213openalex-snapshot

Synergistic Ion‐Pair/Lewis Acid Catalysis Enables Enantioselective Synthesis of Helically Chiral Oxa[6]Helicenes

inferred← citeshttps://doi.org/10.1002/asia.200700415openalex-snapshot

Hydrogen‐Bond‐Mediated Asymmetric Catalysis

inferred← citeshttps://doi.org/10.1002/asia.200800361openalex-snapshot

Chiral Guanidine Catalyzed Enantioselective Reactions

inferred← citeshttps://doi.org/10.1002/asia.201100363openalex-snapshot

Linking Conformational Flexibility and Kinetics: Catalytic 1,4‐Type Friedel–Crafts Reactions of Phenols Utilizing 1,3‐Diamine‐Tethered Guanidine/Bisthiourea Organocatalysts

inferred← citeshttps://doi.org/10.1002/asia.201800493openalex-snapshot

N‐Heterocyclic Carbene (NHC)‐Organocatalyzed Kinetic Resolutions, Dynamic Kinetic Resolutions, and Desymmetrizations

inferred← citeshttps://doi.org/10.1002/bip.22642openalex-snapshot

Site‐selective modification of peptides: From “customizable units” to novel α‐aryl and α‐alkyl glycine derivatives, and components of branched peptides

inferred← citeshttps://doi.org/10.1002/bip.22700openalex-snapshot

Convenient synthesis of collagen‐related tripeptides for segment condensation

inferred← citeshttps://doi.org/10.1002/cbic.201100311openalex-snapshot

Heteromeric Assembled Polypeptidic Artificial Hydrolases with a Six‐Helical Bundle Scaffold

inferred← citeshttps://doi.org/10.1002/cctc.200900301openalex-snapshot

Enantioselective Organocatalytic Strecker Reactions in the Synthesis of α‐Amino Acids

inferred← citeshttps://doi.org/10.1002/cctc.201000413openalex-snapshot

Metallopeptides for Enantioselective Catalysis

inferred← citeshttps://doi.org/10.1002/cctc.201100243openalex-snapshot

The L ‐Leu Hexamer, a Short and Highly Enantioselective Peptide Catalyst for the Juliá–Colonna Epoxidation: Stabilization of a Helical Conformation in DMSO

inferred← citeshttps://doi.org/10.1002/cctc.201300198openalex-snapshot

Powerful Amino Acid Derived Bifunctional Phosphine Catalysts Bearing a Hydrogen Bond Donor in Asymmetric Synthesis

inferred← citeshttps://doi.org/10.1002/cctc.201901246openalex-snapshot

Catalysts Supported by Homochiral Molecular Helices: A New Concept to Implement Asymmetric Amplification in Catalytic Science

inferred← citeshttps://doi.org/10.1002/chem.200800145openalex-snapshot

Organocatalytic Multicomponent α‐Methylenation/Diels–Alder Reactions: A Versatile Route to Substituted Cyclohexenecarbaldehyde Derivatives

inferred← citeshttps://doi.org/10.1002/chem.200901021openalex-snapshot

Tripeptides of the Type H‐ D ‐Pro‐Pro‐Xaa‐NH2 as Catalysts for Asymmetric 1,4‐Addition Reactions: Structural Requirements for High Catalytic Efficiency

inferred← citeshttps://doi.org/10.1002/chem.200901127openalex-snapshot

Bisphosphine‐Functionalized Cyclic Decapeptides Based on the Natural Product Gramicidin S: A Potential Scaffold for Transition‐Metal Coordination

inferred← citeshttps://doi.org/10.1002/chem.200901734openalex-snapshot

An Expeditious Multigram‐Scale Synthesis of Lysine Dendrigraft (DGL) Polymers by Aqueous N ‐Carboxyanhydride Polycondensation

inferred← citeshttps://doi.org/10.1002/chem.201000846openalex-snapshot

Asymmetric Addition of Indoles to Isatins Catalysed by Bifunctional Modified Cinchona Alkaloid Catalysts

inferred← citeshttps://doi.org/10.1002/chem.201002202openalex-snapshot

Enantioselective Synthesis of Coumarins Catalyzed by a Bifunctional Amine–Thiourea Catalyst

inferred← citeshttps://doi.org/10.1002/chem.201100498openalex-snapshot

A Multicatalyst System for the One‐Pot Desymmetrization/Oxidation of meso‐1,2‐Alkane Diols

inferred← citeshttps://doi.org/10.1002/chem.201100672openalex-snapshot

Asymmetric Catalysis with Helical Polymers

inferred← citeshttps://doi.org/10.1002/chem.201101025openalex-snapshot

Catalytic Enantioselective Henry Reactions of Isatins: Application in the Concise Synthesis of (S)‐(−)‐Spirobrassinin

inferred← citeshttps://doi.org/10.1002/chem.201102474openalex-snapshot

Polymer‐Supported Enantioselective Bifunctional Catalysts for Nitro‐Michael Addition of Ketones and Aldehydes

inferred← citeshttps://doi.org/10.1002/chem.201102796openalex-snapshot

From the Feist–Bénary Reaction to Organocatalytic Domino Michael–Alkylation Reactions: Asymmetric Synthesis of 3(2 H)‐Furanones

inferred← citeshttps://doi.org/10.1002/chem.201102847openalex-snapshot

Isothiourea‐Mediated Asymmetric O‐ to C‐Carboxyl Transfer of Oxazolyl Carbonates: Structure–Selectivity Profiles and Mechanistic Studies

inferred← citeshttps://doi.org/10.1002/chem.201104021openalex-snapshot

Hydrogen‐Bond‐Mediated Asymmetric Cascade Reaction of Stable Sulfur Ylides with Nitroolefins: Scope, Application and Mechanism

inferred← citeshttps://doi.org/10.1002/chem.201202264openalex-snapshot

Organocatalyzed Enantioselective Desymmetrization of Diols in the Preparation of Chiral Building Blocks

inferred← citeshttps://doi.org/10.1002/chem.201202504openalex-snapshot

A Highly Enantioselective Synthesis of Functionalized 2,3‐Dihydrofurans by a Modified Feist–Bénary Reaction

inferred← citeshttps://doi.org/10.1002/chem.201304877openalex-snapshot

Ureidopeptide‐Based Brønsted Bases: Design, Synthesis and Application to the Catalytic Enantioselective Synthesis of β‐Amino Nitriles from (Arylsulfonyl)acetonitriles

inferred← citeshttps://doi.org/10.1002/chem.201402373openalex-snapshot

Organocatalyzed Step‐Growth Polymerization through Desymmetrization of Cyclic Anhydrides: Synthesis of Chiral Polyesters

inferred← citeshttps://doi.org/10.1002/chem.201501780openalex-snapshot

Synergistic Stereocontrol in the Enantioselective Ruthenium‐Catalyzed Sulfoxidation of Spirodithiolane‐Indolones

inferred← citeshttps://doi.org/10.1002/chem.201501806openalex-snapshot

Dipeptide‐Derived Multifunctional Quaternary Phosphonium Salt Catalyzed Asymmetric Cyclizations via a Tandem Michael Addition/SN2 Sequence

inferred← citeshttps://doi.org/10.1002/chem.201501831openalex-snapshot

Late‐Stage Peptide Diversification by Bioorthogonal Catalytic CH Arylation at 23 °C in H 2 O

inferred← citeshttps://doi.org/10.1002/chem.201502098openalex-snapshot

Sponge‐Like Behaviour in Isoreticular Cu(Gly‐His‐X) Peptide‐Based Porous Materials

inferred← citeshttps://doi.org/10.1002/chem.201502640openalex-snapshot

Functionality, Effectiveness, and Mechanistic Evaluation of a Multicatalyst‐Promoted Reaction Sequence by Electrospray Ionization Mass Spectrometry

inferred← citeshttps://doi.org/10.1002/chem.201600344openalex-snapshot

Emergent Catalytic Behavior of Self‐Assembled Low Molecular Weight Peptide‐Based Aggregates and Hydrogels

inferred← citeshttps://doi.org/10.1002/chem.201600790openalex-snapshot

Site‐Selective Acylations with Tailor‐Made Catalysts

inferred← citeshttps://doi.org/10.1002/chem.201602624openalex-snapshot

Peptide‐Based Molecular Hydrogels as Supramolecular Protein Mimics

inferred← citeshttps://doi.org/10.1002/chem.201605610openalex-snapshot

Highly Enantioselective α‐Cyanation with 4‐Acetylphenyl Cyanate

inferred← citeshttps://doi.org/10.1002/chem.201700604openalex-snapshot

Bifunctional Tripeptide with a Phosphonic Acid as a Brønsted Acid for Michael Addition: Mechanistic Insights

inferred← citeshttps://doi.org/10.1002/chem.201901221openalex-snapshot

Prospect of Thiazole‐based γ‐Peptide Foldamers in Enamine Catalysis: Exploration of the Nitro‐Michael Addition

inferred← citeshttps://doi.org/10.1002/chem.202001514openalex-snapshot

Prebiotically Plausible Organocatalysts Enabling a Selective Photoredox α‐Alkylation of Aldehydes on the Early Earth

inferred← citeshttps://doi.org/10.1002/chem.202102394openalex-snapshot

Additive and Emergent Catalytic Properties of Dimeric Unnatural Amino Acid Derivatives: Aldol and Conjugate Additions

inferred← citeshttps://doi.org/10.1002/chem.202203002openalex-snapshot

Site‐Selective Acylation of Pyranosides with Immobilized Oligopeptide Catalysts in Flow

inferred← citeshttps://doi.org/10.1002/chin.200816248openalex-snapshot

ChemInform Abstract: Asymmetric Catalysis Mediated by Synthetic Peptides

inferred← citeshttps://doi.org/10.1002/chir.20942openalex-snapshot

Asymmetric Diels–Alder reaction involving chiral benzimidazoles as organocatalysts

inferred← citeshttps://doi.org/10.1002/chir.22055openalex-snapshot

Enantioselective Organocatalytic Michael Addition of Ketones to Alkylidene Malonates

inferred← citeshttps://doi.org/10.1002/chir.22159openalex-snapshot

Asymmetric Allylation of α‐Ketoester‐Derived N‐Benzoylhydrazones Promoted by Chiral Sulfoxides/N‐Oxides Lewis Bases: Highly Enantioselective Synthesis of Quaternary α‐Substituted α‐Allyl‐α‐Amino Acids

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