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Highly Enantioselective Direct Alkylation of Arylacetic Acids with Chiral Lithium Amides as Traceless Auxiliaries
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/adsc.200800154openalex-snapshot
Solid‐Phase Synthesis of [5.5]‐Spiroketals
inferredcites →https://doi.org/10.1002/anie.198102071openalex-snapshot
Functional Groups at Concave Sites: Asymmetric Alkylation of Esters with Very High Stereoselectivity and Reversal of Configuration by Change of Solvent
inferredcites →https://doi.org/10.1002/anie.199507931openalex-snapshot
Benzopyranoisoxazolidines as Chiral Auxiliaries for Asymmetric Synthesis
inferredcites →https://doi.org/10.1002/anie.200702142openalex-snapshot
Acyclic Stereocontrol in the Ireland–Claisen Rearrangement of α‐Branched Esters
inferredcites →https://doi.org/10.1002/anie.201005530openalex-snapshot
Gephyronic Acid, a Missing Link between Polyketide Inhibitors of Eukaryotic Protein Synthesis (Part I): Structural Revision and Stereochemical Assignment of Gephyronic Acid
inferredcites →https://doi.org/10.1016/j.tet.2008.10.048openalex-snapshot
Consecutive sigmatropic rearrangements in the enantioselective total synthesis of (−)-joubertinamine and (−)-mesembrine
inferredcites →https://doi.org/10.1016/s0040-4020(98)00957-0openalex-snapshot
Lithium enediolates and dienediolates of carboxylic acids in synthesis: Alkylation with secondary halides
inferredcites →https://doi.org/10.1016/s0040-4020(99)00872-8openalex-snapshot
Asymmetric alkylation mediated by tricyclic chiral sultam auxiliaries
inferredcites →https://doi.org/10.1016/s0040-4039(00)92870-3openalex-snapshot
Enantioselective alkylation of chiral enolates
inferredcites →https://doi.org/10.1016/s0040-4039(01)80046-0openalex-snapshot
Asymmetric alkylation of carboxyamides by using trans-2,5-disubstituted pyrrolidines as chiral auxiliaries
inferredcites →https://doi.org/10.1016/s0040-4039(01)93810-9openalex-snapshot
Asymmetric alkylation of N-acylsultams: A general route to enantiomerically pure, crystalline C(α,α)-disubstituted carboxylic acid derivatives
inferredcites →https://doi.org/10.1016/s0040-4039(99)00299-3openalex-snapshot
Construction of chiral quaternary carbon centers by asymmetric alkylation of achiral lithium enolates mediated by chiral tetradentate ligands: Stoichiometric and catalytic approaches
inferredcites →https://doi.org/10.1021/ja00098a061openalex-snapshot
Catalytic Asymmetric Benzylation of Achiral Lithium Enolates Using a Chiral Ligand for Lithium in the Presence of an Achiral Ligand
inferredcites →https://doi.org/10.1021/ja00099a076openalex-snapshot
Use of Pseudoephedrine as a Practical Chiral Auxiliary for Asymmetric Synthesis
inferredcites →https://doi.org/10.1021/ja0010002openalex-snapshot
Aggregation and Alkylation of Enolates of 2-Phenyl-α-tetralone and 2,6-Diphenyl-α-tetralone1
inferredcites →https://doi.org/10.1021/ja00178a082openalex-snapshot
New procedure for the direct generation of titanium enolates. Diastereoselective bond constructions with representative electrophiles
inferredcites →https://doi.org/10.1021/ja00263a051openalex-snapshot
Enantioselective deprotonation by chiral lithium amide bases: asymmetric synthesis of trimethylsilyl enol ethers from 4-alkylcyclohexanones
inferredcites →https://doi.org/10.1021/ja00370a050openalex-snapshot
Asymmetric alkylation reactions of chiral imide enolates. A practical approach to the enantioselective synthesis of .alpha.-substituted carboxylic acid derivatives
inferredcites →https://doi.org/10.1021/ja00418a041openalex-snapshot
Asymmetric synthesis of R and S .alpha.-alkylalkanoic acids from metalation and alkylation of chiral 2-oxazolines
inferredcites →https://doi.org/10.1021/ja00986a056openalex-snapshot
Metalated carboxylic acids. I. Alkylation
inferredcites →https://doi.org/10.1021/ja01600a035openalex-snapshot
Alkylations at the α-Carbon of Phenylacetic and Diphenylacetic Acids with Benzyl Chloride and Related Halides by Alkali Amides
inferredcites →https://doi.org/10.1021/ja020816vopenalex-snapshot
Synthesis of the Eight Enantiomerically Pure Diastereomers of the 12-F2-Isoprostanes
inferredcites →https://doi.org/10.1021/ja110192bopenalex-snapshot
Enantioselective Total Synthesis of (+)-Salvileucalin B
inferredcites →https://doi.org/10.1021/ja800435jopenalex-snapshot
Total Synthesis of (+)-Pinnatoxin A
inferredcites →https://doi.org/10.1021/ja970402fopenalex-snapshot
Pseudoephedrine as a Practical Chiral Auxiliary for the Synthesis of Highly Enantiomerically Enriched Carboxylic Acids, Alcohols, Aldehydes, and Ketones
inferredcites →https://doi.org/10.1021/jm0708533openalex-snapshot
Novel Fluorinated Derivatives of the Broad-Spectrum MMP Inhibitors N-Hydroxy-2(R)-[[(4-methoxyphenyl)sulfonyl](benzyl)- and (3-picolyl)-amino]-3-methyl-butanamide as Potential Tools for the Molecular Imaging of Activated MMPs with PET
inferredcites →https://doi.org/10.1021/jo00968a027openalex-snapshot
.alpha. Anions of carboxylic acids. II. Formation and alkylation of .alpha.-metalated aliphatic acids
inferredcites →https://doi.org/10.1021/jo01303a046openalex-snapshot
Asymmetric alkylation of amide anions. Product analysis by GLC using cholesteryl cinnamate, a liquid crystal phase
inferredcites →https://doi.org/10.1021/jo034377+openalex-snapshot
Aggregation and Reactivity of the Dilithium and Dicesium Enediolates of 1-Naphthylacetic Acid1
inferredcites →https://doi.org/10.1021/jo102038qopenalex-snapshot
Synthesis of Methyl N-Boc-(2S,4R)-4-methylpipecolate
inferredcites →https://doi.org/10.1021/ol1031409openalex-snapshot
A Convergent Synthesis of the C1−C16 Segment of Goniodomin A via Palladium-Catalyzed Organostannane−Thioester Coupling
inferredcites →https://doi.org/10.1021/ol200834popenalex-snapshot
Stereoselective Synthesis of a Model C(18)–C(35) Spiroketal Fragment of Integramycin
inferredcites →https://doi.org/10.1021/ol8027797openalex-snapshot
Studies Toward the Synthesis of Spirolides: Assembly of the Elaborated E-Ring Fragment
inferredcites →https://doi.org/10.1021/op0602371openalex-snapshot
Dynamic Biphasic Counterion Exchange in a Configurationally Stable Aziridinium Ion: Efficient Synthesis and Isolation of a Koga C2-Symmetric Tetraamine Base
inferredcites →https://doi.org/10.1039/c39870000656openalex-snapshot
Asymmetric synthesis using chiral bases: enantioselective α-alkylation of carboxylic acids
inferredcites →https://doi.org/10.1055/s-1991-26515openalex-snapshot
Pheromones 80.1Synthesis of (S)-(+)-Manicone and (S)-(+)-Normanicone, Mandibular Gland Constituents of Myrmicine Ants
inferredcites →https://doi.org/10.1248/cpb.45.2122openalex-snapshot
Enantioselective .ALPHA.-Alkylation of Phenylacetic Acid Using a Chiral Bidentate Lithium Amide as a Chiral Auxiliary.
inferredcites →https://doi.org/10.1351/pac199668030691openalex-snapshot
Recent advances in asymmetric synthesis using chiral lithium amide bases
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.4494474openalex-extracted
Catalytic Enantioselective Gilman-Speeter Synthesis of Β-Lactams by Nucleophilic Activation of Carboxylic Acids
inferred← citeshttps://doi.org/10.1002/9780470979525.ch9openalex-snapshot
Carbanions and Electrophilic Aliphatic Substitution
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub6openalex-snapshot
Chiral Auxiliaries and Catalysts
inferred← citeshttps://doi.org/10.1002/9780471264194.fos02343.pub7openalex-snapshot
Chiral Auxiliaries and Catalysts
inferred← citeshttps://doi.org/10.1002/9781118560273.ch9openalex-snapshot
Carbanions and Electrophilic Aliphatic Substitution
inferred← citeshttps://doi.org/10.1002/9781118596784.ssd007openalex-snapshot
Asymmetric α‐Alkylation of Aldehydes, Ketones, and Carboxylic Acids
inferred← citeshttps://doi.org/10.1002/9781118662083.cot09-005openalex-snapshot
Formation of Nitriles, Carboxylic Acids, and Derivatives by Alkylation, Acylation, and Substitution
inferred← citeshttps://doi.org/10.1002/9783527667512.ch10openalex-snapshot
Advances in the Chemistry of Chiral Lithium Amides
inferred← citeshttps://doi.org/10.1002/adsc.201700416openalex-snapshot
Regio‐ and Stereoselective Oxidation of Styrene Derivatives to Arylalkanoic Acids via One‐Pot Cascade Biotransformations
inferred← citeshttps://doi.org/10.1002/adsc.202100006openalex-snapshot
Pyrazoleamides in Catalytic Asymmetric Reactions: Recent Advances
inferred← citeshttps://doi.org/10.1002/ajoc.201900583openalex-snapshot
Arylacetic Acids in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/ange.201105801openalex-snapshot
Palladium‐Catalyzed Allylic Alkylation of Carboxylic Acid Derivatives: N‐Acyloxazolinones as Ester Enolate Equivalents
inferred← citeshttps://doi.org/10.1002/ange.201504113openalex-snapshot
10‐Step Asymmetric Total Synthesis and Stereochemical Elucidation of (+)‐Dragmacidin D
inferred← citeshttps://doi.org/10.1002/ange.201605199openalex-snapshot
Mixed Aggregates of the Dilithiated Koga Tetraamine: NMR Spectroscopic and Computational Studies
inferred← citeshttps://doi.org/10.1002/ange.201703311openalex-snapshot
Katalytische Desymmetrisierung durch C‐H‐Funktionalisierung: eine Lösung für das Problem der stereogenen Methylgruppe
inferred← citeshttps://doi.org/10.1002/ange.201708665openalex-snapshot
Nucleophilic Arylation of N,O‐Ketene Acetals with Triaryl Aluminum Reagents: Access to α‐Aryl Amides through an Umpolung Process
inferred← citeshttps://doi.org/10.1002/ange.201905174openalex-snapshot
Enantioselective Palladium‐Catalyzed Cross‐Coupling of α‐Bromo Carboxamides and Aryl Boronic Acids
inferred← citeshttps://doi.org/10.1002/ange.202000988openalex-snapshot
Oxidation of Alkynyl Boronates to Carboxylic Acids, Esters, and Amides
inferred← citeshttps://doi.org/10.1002/ange.202116136openalex-snapshot
Enantioselective Total Synthesis of Hyperforin and Pyrohyperforin
inferred← citeshttps://doi.org/10.1002/ange.202209987openalex-snapshot
Lithium Enolate with a Lithium‐Alkyne Interaction in the Enantioselective Construction of Quaternary Carbon Centers: Concise Synthesis of (+)‐Goniomitine
inferred← citeshttps://doi.org/10.1002/ange.202400478openalex-snapshot
Enantioselective Synthesis of the 1,3‐Dienyl‐5‐Alkyl‐6‐Oxy Motif: Method Development and Total Synthesis
inferred← citeshttps://doi.org/10.1002/ange.202523659openalex-snapshot
Nickel‐Catalyzed Asymmetric Hydrogenation of All‐Carbon Tetrasubstituted Alkenes Enabled by van der Waals Interactions
inferred← citeshttps://doi.org/10.1002/anie.201105801openalex-snapshot
Palladium‐Catalyzed Allylic Alkylation of Carboxylic Acid Derivatives: N‐Acyloxazolinones as Ester Enolate Equivalents
inferred← citeshttps://doi.org/10.1002/anie.201504113openalex-snapshot
10‐Step Asymmetric Total Synthesis and Stereochemical Elucidation of (+)‐Dragmacidin D
inferred← citeshttps://doi.org/10.1002/anie.201605199openalex-snapshot
Mixed Aggregates of the Dilithiated Koga Tetraamine: NMR Spectroscopic and Computational Studies
inferred← citeshttps://doi.org/10.1002/anie.201703311openalex-snapshot
Catalytic Desymmetrization by C−H Functionalization as a Solution to the Chiral Methyl Problem
inferred← citeshttps://doi.org/10.1002/anie.201708665openalex-snapshot
Nucleophilic Arylation of N , O ‐Ketene Acetals with Triaryl Aluminum Reagents: Access to α‐Aryl Amides through an Umpolung Process
inferred← citeshttps://doi.org/10.1002/anie.201905174openalex-snapshot
Enantioselective Palladium‐Catalyzed Cross‐Coupling of α‐Bromo Carboxamides and Aryl Boronic Acids
inferred← citeshttps://doi.org/10.1002/anie.202000988openalex-snapshot
Oxidation of Alkynyl Boronates to Carboxylic Acids, Esters, and Amides
inferred← citeshttps://doi.org/10.1002/anie.202116136openalex-snapshot
Enantioselective Total Synthesis of Hyperforin and Pyrohyperforin
inferred← citeshttps://doi.org/10.1002/anie.202209987openalex-snapshot
Lithium Enolate with a Lithium‐Alkyne Interaction in the Enantioselective Construction of Quaternary Carbon Centers: Concise Synthesis of (+)‐Goniomitine
inferred← citeshttps://doi.org/10.1002/anie.202400478openalex-snapshot
Enantioselective Synthesis of the 1,3‐Dienyl‐5‐Alkyl‐6‐Oxy Motif: Method Development and Total Synthesis
inferred← citeshttps://doi.org/10.1002/anie.202523659openalex-snapshot
Nickel‐Catalyzed Asymmetric Hydrogenation of All‐Carbon Tetrasubstituted Alkenes Enabled by van der Waals Interactions
inferred← citeshttps://doi.org/10.1002/asia.202201113openalex-snapshot
The Enediolate Chemistry of Free Carboxylic Acids
inferred← citeshttps://doi.org/10.1002/cctc.202500091openalex-snapshot
Photoinduced Direct β‐Allylation of Carboxylic Acids Enabled by Boron Catalysis with a Mixed Two‐Ligand System
inferred← citeshttps://doi.org/10.1002/chem.202104273openalex-snapshot
Copper‐Catalyzed Enantioselective Reductive Aldol Reaction of α,β‐Unsaturated Carboxylic Acids to Alkyl Aryl Ketones: Silanes as Activator and Transient Protecting Group
inferred← citeshttps://doi.org/10.1002/chem.202202575openalex-snapshot
Diastereo‐ and Enantioselective Reductive Mannich‐type Reaction of α,β‐Unsaturated Carboxylic Acids to Ketimines: A Direct Entry to Unprotected β2,3,3‐Amino Acids
inferred← citeshttps://doi.org/10.1002/chin.201202076openalex-snapshot
ChemInform Abstract: Highly Enantioselective Direct Alkylation of Arylacetic Acids with Chiral Lithium Amides as Traceless Auxiliaries.
inferred← citeshttps://doi.org/10.1002/ejoc.201402450openalex-snapshot
Palladium‐Catalyzed α‐Arylation of Carboxylic Acid Derivatives with Grignard Reagent
inferred← citeshttps://doi.org/10.1002/ejoc.201403607openalex-snapshot
A Cascade Aza‐Cope/Aza‐Prins Cyclization Leading to Piperidine Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.202201249openalex-snapshot
Boron Catalysis in the Transformation of Carboxylic Acids and Carboxylic Acid Derivatives
inferred← citeshttps://doi.org/10.1002/slct.73958openalex-snapshot
Organocatalytic Enantioselective Synthesis From Carboxylic Acids via In Situ Activation
inferred← citeshttps://doi.org/10.1002/tcr.202200273openalex-snapshot
Boron‐Catalyzed α‐Functionalizations of Carboxylic Acids
inferred← citeshttps://doi.org/10.1007/s10593-015-1712-7openalex-snapshot
Enantioselective formal synthesis of doxapram
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00301-3openalex-snapshot
3.01 Alkylations of Enols and Enolates
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00153-8openalex-snapshot
Alkylations of Enols and Enolates
inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00064-3openalex-snapshot
One or More CC Bond(s) Formed by Substitution: Substitution of Halogen
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113659openalex-snapshot
Synthetic access to thiolane-based therapeutics and biological activity studies
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Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules
inferred← citeshttps://doi.org/10.1016/j.rechem.2023.101067openalex-snapshot
Catalytic enantioselective Gilman-Speeter synthesis of β-lactams by nucleophilic activation of carboxylic acids
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134463openalex-snapshot
Expanding the library of β-ketoiminates via terminal alkylation of the backbone and their application to the synthesis of unsymmetric 2,4-disubstituted quinolines
inferred← citeshttps://doi.org/10.1016/j.tetasy.2017.04.011openalex-snapshot
2-Cyano-2-indolylpropanoic acid as a chiral derivatizing agent for the absolute configuration assignment of secondary alcohols and primary amines by 1H NMR and VCD
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.08.073openalex-snapshot
Asymmetric alkylation of 5-alkyl-2-aminothiazolones using a C2-symmetric chiral tetraamine base
inferred← citeshttps://doi.org/10.1016/j.xcrp.2024.101822openalex-snapshot
Construction of halogenated tetrasubstituted carbon centers through copper(I)-catalyzed asymmetric alkylation of 2-azaarylesters
inferred← citeshttps://doi.org/10.1021/acs.accounts.0c00709openalex-snapshot
Navigating the Pauson–Khand Reaction in Total Syntheses of Complex Natural Products
inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c00564openalex-snapshot
Catalytic Enantioselective Alkylation of Prochiral Enolates
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.0c00230openalex-snapshot
Achiral Derivatives of Hydroxamate AR-42 Potently Inhibit Class I HDAC Enzymes and Cancer Cell Proliferation
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.9b00497openalex-snapshot
Synthesis of Shld Derivatives, Their Binding to the Destabilizing Domain, and Influence on Protein Accumulation in Transgenic Plants
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00542openalex-snapshot
Total Synthesis of (+)–Haperforin G
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02622openalex-snapshot
Asymmetric Synthesis of γ-Lactones through Koga Amine-Controlled Addition of Enediolates to α,β-Unsaturated Sulfoxonium Salts
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00698openalex-snapshot
An Inexpensive and Scalable Synthesis of Shld
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03366openalex-snapshot
Stereoselective Alkylation of Chiral Titanium(IV) Enolates with tert-Butyl Peresters
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04870openalex-snapshot
Enantioselective Annulation Reactions Enabled by Chiral Lithium Amides as Traceless Auxiliaries
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00914openalex-snapshot
Ligand-Promoted, Boron-Mediated Chemoselective Carboxylic Acid Aldol Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01018openalex-snapshot
Enantioselective Alkylation of Fused Bicyclic Pyridines Enabled by Chiral Lithium Amides as Traceless Auxiliaries
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01978openalex-snapshot
Enantioselective Synthesis of (−)-Aspidospermidine and (+)-Quebrachamine via Chiral Lithium Amide Alkylation of Alkynylacetic Acids
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02945openalex-snapshot
Enantioselective Total Synthesis of Rhodocoranes C, D, and E by Chiral Lithium Amide Alkylation and Gold-Catalyzed Spirocyclization
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01189openalex-snapshot
Determination of the Absolute Configuration of β-Chiral Primary Alcohols Using the Competing Enantioselective Conversion Method
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00587openalex-snapshot
Direct Enantioselective and Regioselective Alkylation of β,γ-Unsaturated Carboxylic Acids with Chiral Lithium Amides as Traceless Auxiliaries
inferred← citeshttps://doi.org/10.1021/acscatal.1c02558openalex-snapshot
Visible-Light-Driven α-Allylation of Carboxylic Acids
inferred← citeshttps://doi.org/10.1021/acscatal.5c07607openalex-snapshot
Asymmetric Organocatalytic Methylation of Prochiral Phosphinic Acids: Construction of P(V)-Stereogenic Centers
inferred← citeshttps://doi.org/10.1021/acscatal.8b00327openalex-snapshot
Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications
inferred← citeshttps://doi.org/10.1021/ja402922wopenalex-snapshot
Catalytic Asymmetric Reductive Acyl Cross-Coupling: Synthesis of Enantioenriched Acyclic α,α-Disubstituted Ketones
inferred← citeshttps://doi.org/10.1021/ja403076uopenalex-snapshot
Enediolate–Dilithium Amide Mixed Aggregates in the Enantioselective Alkylation of Arylacetic Acids: Structural Studies and a Stereochemical Model
inferred← citeshttps://doi.org/10.1021/ja406912hopenalex-snapshot
Mixed Aggregates of an Alkyl Lithium Reagent and a Chiral Lithium Amide Derived from N-Ethyl-O-triisopropylsilyl Valinol
inferred← citeshttps://doi.org/10.1021/ja408856popenalex-snapshot
Electrophilic Rearrangements of Chiral Amides: A Traceless Asymmetric α-Allylation
inferred← citeshttps://doi.org/10.1021/ja4123957openalex-snapshot
Influence of Steric Factors on Chiral Lithium Amide Aggregates
inferred← citeshttps://doi.org/10.1021/ja505179yopenalex-snapshot
Chiral Lithium Diamides Derived from Linked N-Isopropyl Valinol or Alaninol
inferred← citeshttps://doi.org/10.1021/ja506500uopenalex-snapshot
Diastereo- and Enantioselective Iridium-Catalyzed Allylation of Cyclic Ketone Enolates: Synergetic Effect of Ligands and Barium Enolates
inferred← citeshttps://doi.org/10.1021/ja5109084openalex-snapshot
Cobalt–Bisoxazoline-Catalyzed Asymmetric Kumada Cross-Coupling of Racemic α-Bromo Esters with Aryl Grignard Reagents
inferred← citeshttps://doi.org/10.1021/ja512213copenalex-snapshot
Direct Enantioselective Conjugate Addition of Carboxylic Acids with Chiral Lithium Amides as Traceless Auxiliaries
inferred← citeshttps://doi.org/10.1021/jacs.0c10122openalex-snapshot
Total Synthesis of (+)-Haperforin G
inferred← citeshttps://doi.org/10.1021/jacs.1c00249openalex-snapshot
Catalytic Asymmetric Synthesis of Unprotected β2-Amino Acids
inferred← citeshttps://doi.org/10.1021/jacs.4c12154openalex-snapshot
Copper(I)-Catalyzed Enantioselective α-Alkylation of 2-Acylimidazoles
inferred← citeshttps://doi.org/10.1021/jacs.5b04175openalex-snapshot
Chemoselective Boron-Catalyzed Nucleophilic Activation of Carboxylic Acids for Mannich-Type Reactions
inferred← citeshttps://doi.org/10.1021/jacs.5c13977openalex-snapshot
Chiral Lithium Amides as Key Reagents in Enantioselective Synthesis of 2-Alkylpyridines with Multiple Stereocenters
inferred← citeshttps://doi.org/10.1021/jacs.6b01694openalex-snapshot
Uniting C1-Ammonium Enolates and Transition Metal Electrophiles via Cooperative Catalysis: The Direct Asymmetric α-Allylation of Aryl Acetic Acid Esters
inferred← citeshttps://doi.org/10.1021/jacs.6b11673openalex-snapshot
Lithium Enolates in the Enantioselective Construction of Tetrasubstituted Carbon Centers with Chiral Lithium Amides as Noncovalent Stereodirecting Auxiliaries
inferred← citeshttps://doi.org/10.1021/jacs.7b07685openalex-snapshot
Total Synthesis of Unsymmetrically Oxidized Nuphar Thioalkaloids via Copper-Catalyzed Thiolane Assembly
inferred← citeshttps://doi.org/10.1021/jacs.9b08659openalex-snapshot
Enantioselective Alkylation of 2-Alkylpyridines Controlled by Organolithium Aggregation
inferred← citeshttps://doi.org/10.1021/jo400378gopenalex-snapshot
Intermolecular Enantioselective Heck–Matsuda Arylations of Acyclic Olefins: Application to the Synthesis of β-Aryl-γ-lactones and β-Aryl Aldehydes
inferred← citeshttps://doi.org/10.1021/jo400839qopenalex-snapshot
Crystal Structure and Solution State Characterization of Lithium (S)-(1-(Bis(2-methoxyethyl)amino)-3-methylbutan-2-yl)(methyl)amide
inferred← citeshttps://doi.org/10.1038/s41467-023-37967-yopenalex-snapshot
Copper(I)-catalyzed asymmetric alkylation of α-imino-esters
inferred← citeshttps://doi.org/10.1038/s41467-023-40980-wopenalex-snapshot
A biocatalytic platform for asymmetric alkylation of α-keto acids by mining and engineering of methyltransferases
inferred← citeshttps://doi.org/10.1039/c2cc33743fopenalex-snapshot
Enantioselective synthesis of levomilnacipran
inferred← citeshttps://doi.org/10.1039/c2ic90011dopenalex-snapshot
Alkaline and alkaline earth metals
inferred← citeshttps://doi.org/10.1039/c3ic90010jopenalex-snapshot
Alkaline and alkaline earth metals
inferred← citeshttps://doi.org/10.1039/c4cc06895eopenalex-snapshot
The asymmetric alkylation of dimethylhydrazones; intermolecular chirality transfer using sparteine as chiral ligand
inferred← citeshttps://doi.org/10.1039/c4qo00027gopenalex-snapshot
A general method for asymmetric arylation and vinylation of silyl ketene acetals
inferred← citeshttps://doi.org/10.1039/c5ob00402kopenalex-snapshot
Stereogenic α-carbons determine the shape and topology of [13]-macrodilactones
inferred← citeshttps://doi.org/10.1039/c5ra25296bopenalex-snapshot
Metal-free, catalytic regioselective oxidative conversion of vinylarenes: a mild approach to phenylacetic acid derivatives
inferred← citeshttps://doi.org/10.1039/c6ra03303bopenalex-snapshot
Reducing properties of 1,2-dipyridyl-1,2-disodioethanes: chemical validation of theoretical and electrochemical predictions
inferred← citeshttps://doi.org/10.1039/c9sc02678aopenalex-snapshot
Computational design of syntheses leading to compound libraries or isotopically labelled targets
inferred← citeshttps://doi.org/10.1039/d1ob01944aopenalex-snapshot
Synthesis of a TNF inhibitor, flurbiprofen and an i -Pr analogue in enantioenriched forms by copper-catalyzed propargylic substitution with Grignard reagents
inferred← citeshttps://doi.org/10.1039/d1ob02038bopenalex-snapshot
Catalytic asymmetric synthesis of α-stereogenic carboxylic acids: recent advances
inferred← citeshttps://doi.org/10.1039/d1qo01814kopenalex-snapshot
Boron-catalyzed α-C–H fluorination of aryl acetic acids
inferred← citeshttps://doi.org/10.1039/d2gc02204dopenalex-snapshot
Catalyst-free benzylic C(sp 3 )–H cross-coupling with organotrifluoroborates enabled by electrochemistry
inferred← citeshttps://doi.org/10.1039/d2gc04782aopenalex-snapshot
Electrochemical oxidation-induced benzylic C(sp 3 )–H functionalization towards the atom-economic synthesis of oxazole heterocycles
inferred← citeshttps://doi.org/10.1039/d2ob00640eopenalex-snapshot
A facile approach to C -functionalized β-ketoimine compounds via terminal alkylation of a tetralithiated intermediate
inferred← citeshttps://doi.org/10.1039/d3cc06018gopenalex-snapshot
Organocatalytic enantioselective decarboxylative protonation of α-alkyl-α-aryl malonate monoesters
inferred← citeshttps://doi.org/10.1039/d6cc02837copenalex-snapshot
Hydrophobic pocket engineering of arylmalonate decarboxylase expands its substrate scope towards the synthesis of the ( R )-enantiomers of sterically hindered carboxylic acids
inferred← citeshttps://doi.org/10.1055/a-2039-6352openalex-snapshot
Enantioselective [2,3]-Wittig Rearrangement of Carboxylic Acid Derived Enolates by Tetradentate Chiral Lithium Amide
inferred← citeshttps://doi.org/10.1055/a-2640-7673openalex-snapshot
Recent Progress in Enantioselective Alkylation of Metal Enolates
inferred← citeshttps://doi.org/10.1055/a-2900-0552openalex-snapshot
Chiral Lithium Amides: Advancements in Methodology and Applications in Complex Molecule Synthesis
inferred← citeshttps://doi.org/10.1055/sos-sd-120-00214openalex-snapshot
20.2.1.8.15 Synthesis of Carboxylic Acids with Retention of the Functional Group (Update 2024)
inferred← citeshttps://doi.org/10.1248/cpb.c23-00915openalex-snapshot
Development of Efficient Synthetic Reactions Using Enamines and Enamides Carrying Oxygen Atom Substituent on Nitrogen Atom
inferred← citeshttps://doi.org/10.2139/ssrn.4902448openalex-snapshot
Expanding the Library of Β-Ketoiminates Via Terminal Alkylation of the Backbone and Their Application for the Synthesis of Unsymmetric 2,4-Disubstituted Quinolines
inferred← citeshttps://doi.org/10.3390/molecules26164792openalex-snapshot
Recent Advances in the Synthesis of Ibuprofen and Naproxen
inferred← citeshttps://doi.org/10.3987/com-22-14640openalex-snapshot
Supramolecular Chirogenesis in Amide-Linked Bis(Zinc Porphyrin): Application for Absolute Configurational Assignment of Chiral Calboxylic Acids and Chiral Amino Acids
inferred← citeshttps://doi.org/10.4236/ijoc.2014.44026openalex-snapshot
Synthesis of Biotinylated Galiellalactone Analogues
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.82.802openalex-snapshot
Enabling α-Functionalization of Carboxylic Acids by Boron Compounds
inferred← citeshttps://doi.org/10.64898/2026.05.07.723505openalex-snapshot
Hydrophobic pocket engineering of arylmalonate decarboxylase expands its substrate scope towards the synthesis of the ( R )-enantiomers of sterically hindered carboxylic acids
inferred← citeshttps://doi.org/10.70675/e1a3759bz9370z48ddzbd92z1ddf534204f7openalex-snapshot
Synthèse asymétrique de structures cycliques impliquant des composés organométalliques chiraux
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