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Asymmetric Strecker Reactions

https://doi.org/10.1021/cr200057t

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

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Facile and Efficient Enantioselective Strecker Reaction of Ketimines by Chiral Sodium Phosphate

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Helical Chiral Pyridine N‐Oxides: A New Family of Asymmetric Catalysts

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Regioselective Hydration and Deprotection of Chiral, Dissymmetric Iminodinitriles in the Scope of an Asymmetric Strecker Strategy

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Chiral N‐Oxides in Asymmetric Catalysis

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Multicomponent Strecker Reaction under High Pressure

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Chiral Brønsted Acids for Asymmetric Organocatalysis

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Chiral Brønsted Acids for Asymmetric Organocatalysis

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Diastereoselective Strecker reaction of imines derived from D-glyceraldehyde. A new route to β-hydroxy-α-amino acids

inferredcites →https://doi.org/10.1016/0040-4039(95)01377-topenalex-snapshot

Stereoselective Addition of Cyanide Reagents to Nitrones.

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Highly diastereoselective addition of trimethylsilyl cyanide to chiral hydrazones in the presence of Et2AlCl

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Acyclic stereocontrol in the addition of trimethylsilyl cyanide to N-substituted imines of (2S)-lactic aldehyde

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Asymmetric addition of trimethylsilylcyanide to N-benzylimines catalyzed by recyclable chiral dimeric V(V) salen complex

inferredcites →https://doi.org/10.1016/j.tet.2004.06.071openalex-snapshot

Recent advances in asymmetric reactions using sulfinimines (N-sulfinyl imines)

inferredcites →https://doi.org/10.1016/j.tet.2004.07.097openalex-snapshot

A highly enantioselective Strecker reaction catalyzed by titanium-N-salicyl-β-aminoalcohol complexes

inferredcites →https://doi.org/10.1016/j.tet.2004.07.100openalex-snapshot

Asymmetric Strecker reaction of γ-keto acids. Facile entry to α-substituted and α,γ-disubstituted glutamic acids

inferredcites →https://doi.org/10.1016/j.tet.2006.06.107openalex-snapshot

Chiral non-racemic sulfinimines: versatile reagents for asymmetric synthesis

inferredcites →https://doi.org/10.1016/j.tet.2007.06.047openalex-snapshot

Synthesis of new tridentate chiral aminoalcohols by a multicomponent reaction and their evaluation as ligands for catalytic asymmetric Strecker reaction

inferredcites →https://doi.org/10.1016/j.tet.2007.12.002openalex-snapshot

Asymmetric synthesis of β,β-difluoroamino acids via cross-coupling and Strecker reactions

inferredcites →https://doi.org/10.1016/j.tet.2008.05.113openalex-snapshot

New stereoselective synthesis of thiamphenicol and florfenicol from enantiomerically pure cyanohydrin: a chemo-enzymatic approach

inferredcites →https://doi.org/10.1016/j.tet.2008.11.020openalex-snapshot

Organocatalyzed Strecker reactions

inferredcites →https://doi.org/10.1016/j.tet.2009.04.098openalex-snapshot

A practical synthesis of optically active arylglycines via catalytic asymmetric Strecker reaction

inferredcites →https://doi.org/10.1016/j.tetasy.2004.02.032openalex-snapshot

Chiral pyridine N-oxides: useful ligands for asymmetric catalysis

inferredcites →https://doi.org/10.1016/j.tetasy.2006.05.015openalex-snapshot

Catalytic, asymmetric Strecker reactions catalysed by titaniumIV and vanadiumV(salen) complexes

inferredcites →https://doi.org/10.1016/j.tetasy.2006.06.004openalex-snapshot

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inferredcites →https://doi.org/10.1016/j.tetasy.2008.03.013openalex-snapshot

A recyclable chiral auxiliary for the asymmetric syntheses of α-aminonitriles and α-aminophosphinic derivatives

inferredcites →https://doi.org/10.1016/j.tetasy.2008.03.020openalex-snapshot

Experimental and theoretical studies on the asymmetric cyanosilylation of C2-symmetric hydrazones

inferredcites →https://doi.org/10.1016/j.tetasy.2009.01.002openalex-snapshot

Recent progress on the stereoselective synthesis of cyclic quaternary α-amino acids

inferredcites →https://doi.org/10.1016/j.tetlet.2003.09.098openalex-snapshot

Asymmetric Strecker synthesis by addition of trimethylsilyl cyanide to aldehyde SAMP-hydrazones

inferredcites →https://doi.org/10.1016/j.tetlet.2003.09.202openalex-snapshot

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inferredcites →https://doi.org/10.1016/j.tetlet.2004.02.077openalex-snapshot

Catalytic enantioselective Strecker reaction of ketoimines using catalytic amount of TMSCN and stoichiometric amount of HCN

inferredcites →https://doi.org/10.1016/j.tetlet.2004.02.082openalex-snapshot

General and practical catalytic enantioselective Strecker reaction of ketoimines: significant improvement through catalyst tuning by protic additives

inferredcites →https://doi.org/10.1016/j.tetlet.2004.07.034openalex-snapshot

An efficient and practical procedure for Strecker reaction: a highly diastereoselective synthesis of a key intermediate for (+)-biotin

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Enantioselective Strecker-type reaction to sulfonylimines having a 2-pyridylsulfonyl group as a novel stereocontroller

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Advantage of in situ generation of N-arylsulfonyl imines from α-amide sulfones in the phase-transfer-catalyzed asymmetric Strecker reaction

inferredcites →https://doi.org/10.1016/j.tetlet.2007.11.136openalex-snapshot

Fe(Cp)2PF6 catalyzed efficient Strecker reactions of ketones and aldehydes under solvent-free conditions

inferredcites →https://doi.org/10.1016/j.tetlet.2008.04.132openalex-snapshot

Progress toward the synthesis of piperazimycin A: exploration of the synthesis of γ-hydroxy and γ-chloropiperazic acids

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Synthesis of enantiomerically pure ethylenediamines from chiral sulfinimines: a new twist to the Strecker reaction

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Stereoselective cyanosilylation of α-sulfinylketimines or its covalently stabilized enamine tautomers. Synthesis of enantiomerically pure α-sulfinylmethyl-α-amino nitriles

inferredcites →https://doi.org/10.1016/s0040-4020(99)00673-0openalex-snapshot

A simple and efficient diastereoselective Strecker synthesis of optically pure α-arylglycines

inferredcites →https://doi.org/10.1016/s0040-4020(99)01024-8openalex-snapshot

A Chemoenzymatic Access to d- and l-Sphingosines Employing Hydroxynitrile Lyases

inferredcites →https://doi.org/10.1016/s0040-4039(00)78540-6openalex-snapshot

Asymmetric strecker synthesis using enantiopure sulfinimines: A convenient synthesis of α-amino acids

inferredcites →https://doi.org/10.1016/s0040-4039(00)80504-3openalex-snapshot

Reversal of asymmetric induction in stereoselective strecker synthesis on galactosyl amine as the chiral matrix

inferredcites →https://doi.org/10.1016/s0040-4039(00)97719-0openalex-snapshot

Electron-transfer activation. Photocyanation of tertiary amines.

inferredcites →https://doi.org/10.1016/s0040-4039(01)80738-3openalex-snapshot

Asymmetric syntheses of amino acids by addition of cyanide to the schiff bases in the presence of cyanide-modified hemin-copolymer

inferredcites →https://doi.org/10.1016/s0040-4039(02)02270-0openalex-snapshot

High pressure mediated three component Strecker synthesis of α-aminonitriles from ketones, aromatic amines and trimethylsilyl cyanide

inferredcites →https://doi.org/10.1016/s0040-4039(02)02598-4openalex-snapshot

Effect of pressure on the Strecker synthesis of hindered α-aminonitriles from ketones and aromatic amines

inferredcites →https://doi.org/10.1016/s0040-4039(03)00735-4openalex-snapshot

N-Salicyl-β-aminoalcohols as a new class of ligand for catalytic asymmetric Strecker reactions

inferredcites →https://doi.org/10.1016/s0040-4039(99)02215-7openalex-snapshot

Asymmetric Strecker reactions of ketimines catalysed by titanium-based complexes

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Asymmetric synthesis of (2R,3S)-4-halo-3-benzyloxy-2-(N-methoxycarbonyl-N-benzylamino)butyronitriles as precursors for the synthesis of β-hydroxy-α-amino acids

inferredcites →https://doi.org/10.1016/s0957-4166(00)00324-4openalex-snapshot

Enhancement of the diastereoselectivity in the addition of trimethylsilyl cyanide to chiral aldimines by catalysis with a chiral 1,2-diamine: unexpected mechanistic results

inferredcites →https://doi.org/10.1016/s0957-4166(00)80518-2openalex-snapshot

Stereoselective synthesis of β-hydroxy-α-amino acids from chiral cyanohydrins.

inferredcites →https://doi.org/10.1016/s0957-4166(01)00144-6openalex-snapshot

Sc(BINOL)2Li: a new heterobimetallic catalyst for the asymmetric Strecker reaction

inferredcites →https://doi.org/10.1016/s0957-4166(02)00832-7openalex-snapshot

A comparative study of the stereoselective addition of trimethylsilyl cyanide and diethylaluminum cyanide to chiral cyclic nitrones

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Chiral N , N ′-Dioxides: New Ligands and Organocatalysts for Catalytic Asymmetric Reactions

inferredcites →https://doi.org/10.1021/cr0000630openalex-snapshot

Use of Achiral and Meso Ligands To Convey Asymmetry in Enantioselective Catalysis

inferredcites →https://doi.org/10.1021/cr00013a009openalex-snapshot

The chiral pool as a source of enantioselective catalysts and auxiliaries

inferredcites →https://doi.org/10.1021/cr000260zopenalex-snapshot

Symmetry Breaking in Asymmetric Catalysis: Racemic Catalysis to Autocatalysis

inferredcites →https://doi.org/10.1021/cr0200318openalex-snapshot

Chiral Poisoning and Asymmetric Activation

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

Catalytic Enantioselective Strecker Reactions and Analogous Syntheses

inferredcites →https://doi.org/10.1021/cr050580oopenalex-snapshot

Catalytic Asymmetric Synthesis of α-Amino Acids

inferredcites →https://doi.org/10.1021/cr068374jopenalex-snapshot

Stronger Brønsted Acids

inferredcites →https://doi.org/10.1021/ja0010352openalex-snapshot

Asymmetric Reissert-type Reaction Promoted by Bifunctional Catalyst

inferredcites →https://doi.org/10.1021/ja010654nopenalex-snapshot

Catalytic Enantioselective Reissert-Type Reaction: Development and Application to the Synthesis of a Potent NMDA Receptor Antagonist (−)-L-689,560 Using a Solid-Supported Catalyst

inferredcites →https://doi.org/10.1021/ja016682nopenalex-snapshot

Switching Enantiofacial Selectivities Using One Chiral Source: Catalytic Enantioselective Synthesis of the Key Intermediate for (20S)-Camptothecin Family by (S)-Selective Cyanosilylation of Ketones

inferredcites →https://doi.org/10.1021/ja016935copenalex-snapshot

Enantioselective Construction of Quaternary Stereocenter through a Reissert-Type Reaction Catalyzed by an Electronically Tuned Bifunctional Catalyst: Efficient Synthesis of Various Biologically Significant Compounds

inferredcites →https://doi.org/10.1021/ja025848xopenalex-snapshot

Asymmetric Diels−Alder Reactions Catalyzed by a Triflic Acid Activated Chiral Oxazaborolidine

inferredcites →https://doi.org/10.1021/ja027246jopenalex-snapshot

Structure-Based Analysis and Optimization of a Highly Enantioselective Catalyst for the Strecker Reaction

inferredcites →https://doi.org/10.1021/ja027468hopenalex-snapshot

Broad-Spectrum Enantioselective Diels−Alder Catalysis by Chiral, Cationic Oxazaborolidines

inferredcites →https://doi.org/10.1021/ja034980+openalex-snapshot

Catalytic Enantioselective Strecker Reaction of Ketoimines

inferredcites →https://doi.org/10.1021/ja035393ropenalex-snapshot

Triflimide Activation of a Chiral Oxazaborolidine Leads to a More General Catalytic System for Enantioselective Diels−Alder Addition

inferredcites →https://doi.org/10.1021/ja045966fopenalex-snapshot

New Entries in Lewis Acid−Lewis Base Bifunctional Asymmetric Catalyst: Catalytic Enantioselective Reissert Reaction of Pyridine Derivatives

inferredcites →https://doi.org/10.1021/ja046154mopenalex-snapshot

Application of Chiral Cationic Catalysts to Several Classical Syntheses of Racemic Natural Products Transforms Them into Highly Enantioselective Pathways

inferredcites →https://doi.org/10.1021/ja0475959openalex-snapshot

Highly Enantioselective Cyanosilylation of Aldehydes Catalyzed by a Chiral Oxazaborolidinium Ion

inferredcites →https://doi.org/10.1021/ja0491533openalex-snapshot

Chiral Brønsted Acid-Catalyzed Direct Mannich Reactions via Electrophilic Activation

inferredcites →https://doi.org/10.1021/ja049323bopenalex-snapshot

Enantioselective and Structure-Selective Diels−Alder Reactions of Unsymmetrical Quinones Catalyzed by a Chiral Oxazaborolidinium Cation. Predictive Selection Rules

inferredcites →https://doi.org/10.1021/ja050543eopenalex-snapshot

Enantioselective Cyanosilylation of Ketones Catalyzed by a Chiral Oxazaborolidinium Ion

inferredcites →https://doi.org/10.1021/ja058066nopenalex-snapshot

Asymmetric Strecker Reaction of Aldimines Using Aqueous Potassium Cyanide by Phase-Transfer Catalysis of Chiral Quaternary Ammonium Salts with a Tetranaphthyl Backbone

inferredcites →https://doi.org/10.1021/ja060841ropenalex-snapshot

Assembly State of Catalytic Modules as Chiral Switches in Asymmetric Strecker Amino Acid Synthesis

inferredcites →https://doi.org/10.1021/ja806875copenalex-snapshot

Pyridinium 1,1′-Binaphthyl-2,2′-disulfonates as Highly Effective Chiral Brønsted Acid−Base Combined Salt Catalysts for Enantioselective Mannich-Type Reaction

inferredcites →https://doi.org/10.1021/ja808715jopenalex-snapshot

Mechanism of BINOL−Phosphoric Acid-Catalyzed Strecker Reaction of Benzyl Imines

inferredcites →https://doi.org/10.1021/ja9058958openalex-snapshot

Mechanism of Amido-Thiourea Catalyzed Enantioselective Imine Hydrocyanation: Transition State Stabilization via Multiple Non-Covalent Interactions

inferredcites →https://doi.org/10.1021/ja907268gopenalex-snapshot

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Catalytic Asymmetric Synthesis of Unnatural Axially Chiral Biaryl δ‐Amino Acid Derivatives via a Chiral Phenanthroline‐Potassium Catalyst‐Enabled Dynamic Kinetic Resolution

inferred← citeshttps://doi.org/10.1002/ange.202408886openalex-snapshot

Direct Asymmetric Synthesis of α‐Aminoimines from 1,2‐Bis‐N‐Sulfinylimines by Using Allyl Boronic Acids

inferred← citeshttps://doi.org/10.1002/ange.202416042openalex-snapshot

Organocatalytic Asymmetric Construction of 2,6‐Diazabicyclo‐[2.2.2]octanes by Harnessing the Potential of an 3‐Oxindolium Ion Intermediate

inferred← citeshttps://doi.org/10.1002/ange.202422185openalex-snapshot

Enzymatic Cascades for Stereoselective and Regioselective Amide Bond Assembly

inferred← citeshttps://doi.org/10.1002/ange.202510811openalex-snapshot

Accessing N ‐Unprotected Unnatural α‐Amino Acid Esters by Half‐Sandwich Chiral‐at‐Ruthenium Aldehyde Catalysis: Scope and Mechanistic Study

inferred← citeshttps://doi.org/10.1002/ange.202511466openalex-snapshot

Direct Synthesis of Amino Acids from Plastic, Air, and Water

inferred← citeshttps://doi.org/10.1002/ange.5717711openalex-snapshot

Selective Glycine Electrosynthesis via C‐N Coupling Enabled by Synergistic Mott–Schottky Heterojunction and Oxygen Vacancies

inferred← citeshttps://doi.org/10.1002/anie.201206755openalex-snapshot

Copper‐Catalyzed Amination of Ketene Silyl Acetals with Hydroxylamines: Electrophilic Amination Approach to α‐Amino Acids

inferred← citeshttps://doi.org/10.1002/anie.201300231openalex-snapshot

Acid‐Catalyzed In Situ Generation of Less Accessible or Unprecedented N ‐Boc Imines from N ‐Boc Aminals

inferred← citeshttps://doi.org/10.1002/anie.201303572openalex-snapshot

Enantioselective Cyanoethoxycarbonylation of Isatins Promoted by a Lewis Base–Brønsted Acid Cooperative Catalyst

inferred← citeshttps://doi.org/10.1002/anie.201407677openalex-snapshot

Asymmetric Triple Relay Catalysis: Enantioselective Synthesis of Spirocyclic Indolines through a One‐Pot Process Featuring an Asymmetric 6π Electrocyclization

inferred← citeshttps://doi.org/10.1002/anie.201502215openalex-snapshot

Versatile In Situ Generated N ‐Boc‐Imines: Application to Phase‐Transfer‐Catalyzed Asymmetric Mannich‐Type Reactions

inferred← citeshttps://doi.org/10.1002/anie.201508371openalex-snapshot

Highly Enantioselective Aza‐Michael Reaction between Alkyl Amines and β‐Trifluoromethyl β‐Aryl Nitroolefins

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.201806874openalex-snapshot

Selective and Catalytic Hydrocarboxylation of Enamides and Imines with CO 2 to Generate α,α‐Disubstituted α‐Amino Acids

inferred← citeshttps://doi.org/10.1002/anie.201809310openalex-snapshot

A General Amino Acid Synthesis Enabled by Innate Radical Cross‐Coupling

inferred← citeshttps://doi.org/10.1002/anie.201909919openalex-snapshot

Consecutive Intermolecular Reductive Amination/Asymmetric Hydrogenation: Facile Access to Sterically Tunable Chiral Vicinal Diamines and N‐Heterocyclic Carbenes

inferred← citeshttps://doi.org/10.1002/anie.201910864openalex-snapshot

Regiodivergent Intramolecular Nucleophilic Addition of Ketimines for the Diverse Synthesis of Azacycles

inferred← citeshttps://doi.org/10.1002/anie.201914797openalex-snapshot

Hydrogen Bond Assisted l to d Conversion of α‐Amino Acids

inferred← citeshttps://doi.org/10.1002/anie.202010157openalex-snapshot

Radical‐Based Synthesis and Modification of Amino Acids

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.202015898openalex-snapshot

Enantioselective Reductive Cyanation and Phosphonylation of Secondary Amides by Iridium and Chiral Thiourea Sequential Catalysis

inferred← citeshttps://doi.org/10.1002/anie.202016667openalex-snapshot

Chemical Conversion and Locking of the Imine Linkage: Enhancing the Functionality of Covalent Organic Frameworks

inferred← citeshttps://doi.org/10.1002/anie.202101517openalex-snapshot

Catalytic Diastereo‐ and Enantioconvergent Synthesis of Vicinal Diamines from Diols through Borrowing Hydrogen

inferred← citeshttps://doi.org/10.1002/anie.202102864openalex-snapshot

Electrophilic Aminating Agents in Total Synthesis

inferred← citeshttps://doi.org/10.1002/anie.202115435openalex-snapshot

Leveraging Electron‐Deficient Iminium Intermediates in a General Synthesis of Valuable Amines

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.202207153openalex-snapshot

Umpolung Ala B Reagents for the Synthesis of Non‐Proteogenic Amino Acids, Peptides and Proteins**

inferred← citeshttps://doi.org/10.1002/anie.202210755openalex-snapshot

Modular Construction of Unnatural α‐Tertiary Amino Acid Derivatives by Multicomponent Radical Cross‐Couplings

inferred← citeshttps://doi.org/10.1002/anie.202217918openalex-snapshot

Photocatalytic Carboxylation of C−N Bonds in Cyclic Amines with CO2 by Consecutive Visible‐Light‐Induced Electron Transfer

inferred← citeshttps://doi.org/10.1002/anie.202309274openalex-snapshot

Light‐Induced Metal‐Free Generation of Cyanocarbenes from Alkynyl Triazenes for the Synthesis of Nitrile Derivatives

inferred← citeshttps://doi.org/10.1002/anie.202309868openalex-snapshot

Enantioselective Synthesis of Arylglycines via Pd‐Catalyzed Coupling of Schöllkopf Bis‐Lactim Ethers with Aryl Chlorides

inferred← citeshttps://doi.org/10.1002/anie.202403401openalex-snapshot

Atropisomeric Carboxylic Acids Synthesis via Nickel‐Catalyzed Enantioconvergent Carboxylation of Aza‐Biaryl Triflates with CO 2

inferred← citeshttps://doi.org/10.1002/anie.202407920openalex-snapshot

Catalytic Asymmetric Synthesis of Unnatural Axially Chiral Biaryl δ‐Amino Acid Derivatives via a Chiral Phenanthroline‐Potassium Catalyst‐Enabled Dynamic Kinetic Resolution

inferred← citeshttps://doi.org/10.1002/anie.202408886openalex-snapshot

Direct Asymmetric Synthesis of α‐Aminoimines from 1,2‐Bis‐N‐Sulfinylimines by Using Allyl Boronic Acids

inferred← citeshttps://doi.org/10.1002/anie.202416042openalex-snapshot

Organocatalytic Asymmetric Construction of 2,6‐Diazabicyclo‐[2.2.2]octanes by Harnessing the Potential of an 3‐Oxindolium Ion Intermediate

inferred← citeshttps://doi.org/10.1002/anie.202422185openalex-snapshot

Enzymatic Cascades for Stereoselective and Regioselective Amide Bond Assembly

inferred← citeshttps://doi.org/10.1002/anie.202510811openalex-snapshot

Accessing N ‐Unprotected Unnatural α‐Amino Acid Esters by Half‐Sandwich Chiral‐at‐Ruthenium Aldehyde Catalysis: Scope and Mechanistic Study

inferred← citeshttps://doi.org/10.1002/anie.202511466openalex-snapshot

Direct Synthesis of Amino Acids from Plastic, Air, and Water

inferred← citeshttps://doi.org/10.1002/anie.5717711openalex-snapshot

Selective Glycine Electrosynthesis via C‐N Coupling Enabled by Synergistic Mott–Schottky Heterojunction and Oxygen Vacancies

inferred← citeshttps://doi.org/10.1002/aoc.3443openalex-snapshot

Design, synthesis, characterization and catalytic performance of a new cellulose‐based magnetic nanocomposite in the one‐pot three‐component synthesis of α‐aminonitriles

inferred← citeshttps://doi.org/10.1002/aoc.4188openalex-snapshot

Magnetically separable g‐C3N4 hybrid nanocomposite: Highly efficient and eco‐friendly recyclable catalyst for one‐pot synthesis of α‐aminonitriles

inferred← citeshttps://doi.org/10.1002/aoc.4616openalex-snapshot

A unique combination of KI/ZnFe2O4 as a catalyst for oxidative Strecker reaction

inferred← citeshttps://doi.org/10.1002/asia.201200289openalex-snapshot

Ethylene Glycol: A Powerful Catalyst‐Free Medium for CC Bond‐Forming Reactions

inferred← citeshttps://doi.org/10.1002/asia.201300960openalex-snapshot

Ag‐Promoted Azido‐Carbocyclization of Activated Alkenes via CH Bond Cleavage

inferred← citeshttps://doi.org/10.1002/asia.202300805openalex-snapshot

Photoredox Metal‐Free Synthesis of Unnatural β‐Silyl‐α‐Amino Acids via Hydrosilylation

inferred← citeshttps://doi.org/10.1002/cbic.202100661openalex-snapshot

A Four‐Step Enzymatic Cascade for Efficient Production of L‐Phenylglycine from Biobased L‐Phenylalanine

inferred← citeshttps://doi.org/10.1002/cctc.201200617openalex-snapshot

Asymmetric Cyanoethoxy Carbonylation Reaction of Aldehydes Catalyzed by a TiIV Macrocyclic Complex: An Efficient Synthetic Protocol for β‐Blocker and α1‐Adrenergic Receptor Agonists

inferred← citeshttps://doi.org/10.1002/cctc.201200700openalex-snapshot

Catalysis of Enantioselective Strecker Reaction in the Synthesis of D ‐Homophenylalanine Using Recyclable, Chiral, Macrocyclic MnIII–Salen Complexes

inferred← citeshttps://doi.org/10.1002/cctc.201300050openalex-snapshot

Isatin as a Strategic Motif for Asymmetric Catalysis

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

Asymmetric Hydrocyanation of Nitroolefins Catalyzed by an Aluminum(III) Salen Complex

inferred← citeshttps://doi.org/10.1002/cctc.201601144openalex-snapshot

Applications of Chiral Thiourea‐Amine/Phosphine Organocatalysts in Catalytic Asymmetric Reactions

inferred← citeshttps://doi.org/10.1002/cctc.201701068openalex-snapshot

Engineered Aminotransferase for the Production of d ‐Phenylalanine Derivatives Using Biocatalytic Cascades

inferred← citeshttps://doi.org/10.1002/cctc.202000652openalex-snapshot

Palladium‐Catalyzed Decarboxylative Three‐Component Synthesis of α‐Arylglycines: Replacing Boronic with Carboxylic Acids in the Petasis Reaction

inferred← citeshttps://doi.org/10.1002/cctc.202001921openalex-snapshot

Asymmetric Hydrocyanation of N ‐Phosphinoyl Aldimines with Acetone Cyanohydrin by Cooperative Lewis Acid/Onium Salt/Brønsted Base Catalysis

inferred← citeshttps://doi.org/10.1002/cctc.202500258openalex-snapshot

Photoinduced Copper‐Catalyzed Asymmetric Radical Sulfonylcyanation of Vinylarenes with Sulfonyl Cyanides

inferred← citeshttps://doi.org/10.1002/chem.201200528openalex-snapshot

Self‐Supported Chiral Titanium Cluster (SCTC) as a Robust Catalyst for the Asymmetric Cyanation of Imines under Batch and Continuous Flow at Room Temperature

inferred← citeshttps://doi.org/10.1002/chem.201202237openalex-snapshot

A Theoretical Investigation on the Strecker Reaction Catalyzed by a Ti IV ‐Complex Catalyst Generated from a Cinchona Alkaloid, Achiral Substituted 2,2′‐Biphenol, and Tetraisopropyl Titanate

inferred← citeshttps://doi.org/10.1002/chem.201301591openalex-snapshot

Base‐Dependent Stereodivergent Intramolecular Aza‐Michael Reaction: Asymmetric Synthesis of 1,3‐Disubstituted Isoindolines

inferred← citeshttps://doi.org/10.1002/chem.201302007openalex-snapshot

Oxazoline‐Based Organocatalyst for Enantioselective Strecker Reactions: A Protocol for the Synthesis of Levamisole

inferred← citeshttps://doi.org/10.1002/chem.201400117openalex-snapshot

NIS‐Assisted Aza‐Friedel–Crafts Reaction with α‐Carbamoysulfides as Precursors of N‐Carbamoylimines

inferred← citeshttps://doi.org/10.1002/chem.201503243openalex-snapshot

Facile Alder‐Ene Reactions of Silylallenes Involving an Allenic C(sp2)H Bond

inferred← citeshttps://doi.org/10.1002/chem.201603057openalex-snapshot

Mechanochemical Strecker Reaction: Access to α‐Aminonitriles and Tetrahydroisoquinolines under Ball‐Milling Conditions

inferred← citeshttps://doi.org/10.1002/chem.201604914openalex-snapshot

Bismuth Perfluoroalkylphosphinates: New Catalysts for Application in Organic Syntheses

inferred← citeshttps://doi.org/10.1002/chem.201703479openalex-snapshot

Organocatalytic Highly Regio‐ and Enantioselective Umpolung Michael Addition Reaction of α‐Imino Esters

inferred← citeshttps://doi.org/10.1002/chem.201704033openalex-snapshot

Highly Stereoselective Strecker Synthesis Induced by a Slight Modification of Benzhydrylamine from Achiral to Chiral

inferred← citeshttps://doi.org/10.1002/chem.201900531openalex-snapshot

Ruthenium‐Catalyzed Deaminative Hydrogenation of Amino Nitriles: Direct Access to 1,2‐Amino Alcohols

inferred← citeshttps://doi.org/10.1002/chem.202100902openalex-snapshot

Transition‐Metal‐Free α Csp3−H Cyanation of Sulfonamides

inferred← citeshttps://doi.org/10.1002/chem.202201994openalex-snapshot

Asymmetric Alkylation of Cyclic Ketones with Dehydroalanine via H‐Bond‐Directing Enamine Catalysis: Straightforward Access to Enantiopure Unnatural α‐Amino Acids

inferred← citeshttps://doi.org/10.1002/chem.202302061openalex-snapshot

Multiple Hydrogen‐Bonding Catalysts Enhance the Asymmetric Cyanation of Ketimines and Aldimines

inferred← citeshttps://doi.org/10.1002/chem.202402488openalex-snapshot

H‐Bond Donor‐Directed Switch of Diastereoselectivity in the Enantioselective Intramolecular Aza‐Henry Reaction of Ketimines

inferred← citeshttps://doi.org/10.1002/chem.202502272openalex-snapshot

Pd(II)‐Catalyzed Strategies for the β‐Arylation of α‐Amino Acids: An Overview

inferred← citeshttps://doi.org/10.1002/chem.202503359openalex-snapshot

Synthetic Studies Towards Darobactin A

inferred← citeshttps://doi.org/10.1002/chem.71380openalex-snapshot

Electrosynthesis of Glycine From Nitrate and Glyoxylic Acid Over a Bi 2 S 3 Nanosheets‐Based Catalyst

inferred← citeshttps://doi.org/10.1002/chin.201205254openalex-snapshot

ChemInform Abstract: Asymmetric Strecker Reactions

inferred← citeshttps://doi.org/10.1002/chir.23350openalex-snapshot

Comparative study of different chiral ligands for dynamic kinetic resolution of amino acids

inferred← citeshttps://doi.org/10.1002/cjoc.201800001openalex-snapshot

Internally Reuse Waste: Catalytic Asymmetric One‐Pot Strecker Reaction of Fluoroalkyl Ketones, Anilines and TMSCN by Sequential Catalysis

inferred← citeshttps://doi.org/10.1002/cjoc.202400774openalex-snapshot

Asymmetric Synthesis of Chiral Aliphatic α‐Tertiary Aminonitriles via Organocatalytic Isomerization of Cyanoketimines

inferred← citeshttps://doi.org/10.1002/cssc.202400166openalex-snapshot

Alkaline Modified Mesoporous Silica Supported Ruthenium Catalyst for Improved α‐Amino Acid Synthesis

inferred← citeshttps://doi.org/10.1002/cssc.202501255openalex-snapshot

Three‐Step One‐Pot Photocatalytic Oxidation of Feedstocks and Organocatalytic Sequential Cascade to Access Enantioenriched α‐Aminonitriles

inferred← citeshttps://doi.org/10.1002/ejoc.201101073openalex-snapshot

Mimicking Nature to Make Unnatural Amino Acids and Chiral Diamines

inferred← citeshttps://doi.org/10.1002/ejoc.201200030openalex-snapshot

Recent Advances in Asymmetric Isocyanide‐Based Multicomponent Reactions

inferred← citeshttps://doi.org/10.1002/ejoc.201201533openalex-snapshot

Asymmetric Strecker Reaction with Chiral Amines: a Catalyst‐Free Protocol Using Acetone Cyanohydrin in Water

inferred← citeshttps://doi.org/10.1002/ejoc.201201637openalex-snapshot

Solvent‐Assisted Diastereoselective Trimethylsilyl Cyanide Additions to Cyclic α‐Fluoro Ketones

inferred← citeshttps://doi.org/10.1002/ejoc.201201701openalex-snapshot

Chiral α‐Arylethanamines: An Organocatalyst for the Enantioselective α‐Amination of Branched Aldehydes

inferred← citeshttps://doi.org/10.1002/ejoc.201300406openalex-snapshot

Highly Efficient Asymmetric Conjugate Hydrocyanation of Aromatic Enones by an Anionic Chiral Phosphate Catalyst

inferred← citeshttps://doi.org/10.1002/ejoc.201301349openalex-snapshot

Iron‐Catalyzed Three‐Component Synthesis of α‐Amino Acid Derivatives

inferred← citeshttps://doi.org/10.1002/ejoc.201400040openalex-snapshot

Three‐Component Synthesis of α‐Amino‐α‐aryl Carbonitriles from Arynes, Aroyl Cyanides, and N,N‐Dimethylformamide

inferred← citeshttps://doi.org/10.1002/ejoc.201402764openalex-snapshot

Organocatalytic Enantioselective Strecker Reaction of Imines Containing a Thiazole Moiety by Using a Cinchona‐Based Squaramide Catalyst

inferred← citeshttps://doi.org/10.1002/ejoc.201500086openalex-snapshot

Insight into O2‐Promoted Base‐Catalyzed N‐Alkylation of Amines with Alcohols

inferred← citeshttps://doi.org/10.1002/ejoc.201500300openalex-snapshot

Flow Synthesis of Fluorinated α‐Amino Acids

inferred← citeshttps://doi.org/10.1002/ejoc.201800896openalex-snapshot

Site‐Selective C–H Bond Activation/Functionalization of Alpha‐Amino Acids and Peptide‐Like Derivatives

inferred← citeshttps://doi.org/10.1002/ejoc.201801087openalex-snapshot

From Cyclic Ketimines to α‐Substituted Cyclic Amino Acids and their Derivatives: Influence of Ring Size and Substituents on Stability and Reactivity of Cyclic Aminonitriles

inferred← citeshttps://doi.org/10.1002/ejoc.201801170openalex-snapshot

Verkade's Superbase as an Organocatalyst for the Strecker Reaction

inferred← citeshttps://doi.org/10.1002/ejoc.202001650openalex-snapshot

Copper‐Catalyzed Three‐Component Reactions of 2‐Iodo‐2,2‐difluoroacetophenones, Alkynes, and Trimethylsilyl Cyanide

inferred← citeshttps://doi.org/10.1002/ejoc.202200137openalex-snapshot

Synthesis and Application of Monofluoroalkyl Building Blocks: α‐Halo‐α‐fluoroketones

inferred← citeshttps://doi.org/10.1002/ejoc.202200859openalex-snapshot

Radical‐Mediated C−H Alkylation of Glycine Derivatives: A Straightforward Strategy for Diverse α‐Unnatural Amino Acids

inferred← citeshttps://doi.org/10.1002/ejoc.202300736openalex-snapshot

Salicylaldehydes in Strecker Reaction: Synthesis of Tricyclic Benzofuro[2,3‐b]pyrazin‐2(1H)‐ones via One‐Pot Seven Domino Reactions

inferred← citeshttps://doi.org/10.1002/ejoc.202400995openalex-snapshot

Transition‐Metal‐Catalyzed Construction of Axially Chiral Carbonyl Compounds

inferred← citeshttps://doi.org/10.1002/ejoc.202401299openalex-snapshot

Recent Advances in the Synthesis of Amino Acid Derivatives through Multicomponent Reactions

inferred← citeshttps://doi.org/10.1002/ejoc.202401477openalex-snapshot

Blue‐Light‐Induced Stereoselective Synthesis of α ‐Alkylated Amino Acid Derivatives

inferred← citeshttps://doi.org/10.1002/ejoc.202500624openalex-snapshot

Synthesis of Diverse β,β‐Diaryl β‐Siloxy Diamines and Application as Organocatalysts

inferred← citeshttps://doi.org/10.1002/ghg.1279openalex-snapshot

What chemicals will we need to capture CO2?

inferred← citeshttps://doi.org/10.1002/jhet.3582openalex-snapshot

Synthesis of α‐Aminonitriles and 5‐Substituted 1H‐Tetrazoles Using an Efficient Nanocatalyst of Fe3O4@SiO2–APTES‐supported Trifluoroacetic Acid

inferred← citeshttps://doi.org/10.1002/jlcr.3502openalex-snapshot

Synthesis of 2 C‐14 labeled cathepsin C inhibitors: The use of a cyanide to displace a Benzotriazole

inferred← citeshttps://doi.org/10.1002/jps.24667openalex-snapshot

Artifacts Generated During Azoalkane Peroxy Radical Oxidative Stress Testing of Pharmaceuticals Containing Primary and Secondary Amines

inferred← citeshttps://doi.org/10.1002/macp.202000347openalex-snapshot

Rational Optimization of the Petasis Three‐Component Reaction as a Feasible Elementary Reaction in Polymer Chemistry

inferred← citeshttps://doi.org/10.1002/open.202500389openalex-snapshot

Buffer‐Mediated Catalyst‐Free Strecker Reaction Toward Enzymatic Implementation

inferred← citeshttps://doi.org/10.1002/slct.201702850openalex-snapshot

Quinine Thiourea Immobilized on SBA‐15 as an Efficient Recyclable Catalyst for Asymmetric Strecker Reaction of Isatin N ‐protected Ketimines

inferred← citeshttps://doi.org/10.1002/slct.201800113openalex-snapshot

Enantioselective Addition of Cyanide to CF 3 ‐Substituted Alkylidenemalonates: Construction of Trifluoromethylated All‐Carbon Quaternary Stereocenters

inferred← citeshttps://doi.org/10.1002/slct.202002021openalex-snapshot

Cobalt‐Catalyzed Multi‐Component Reactions: Recent Advances and Perspectives in Organic Synthesis

inferred← citeshttps://doi.org/10.1002/slct.202305233openalex-snapshot

Humic Acid: A Promising and Green Bioorganic Catalyst in Organic Syntheses

inferred← citeshttps://doi.org/10.1002/tcr.201600140openalex-snapshot

Squaramide‐Catalyzed Asymmetric Reactions

inferred← citeshttps://doi.org/10.1002/tcr.201800005openalex-snapshot

Chemistry of Cyanide Adducts of Aldimines from Aniline Derivatives

inferred← citeshttps://doi.org/10.1002/tcr.202000066openalex-snapshot

‐Aminonitriles: From Sustainable Preparation to Applications in Natural Product Synthesis

inferred← citeshttps://doi.org/10.1007/7081_2015_187openalex-snapshot

Synthesis of Peptidomimetics Through the Disrupted Ugi Reaction with Aziridine Aldehyde Dimers

inferred← citeshttps://doi.org/10.1007/978-3-319-49119-6openalex-snapshot

Peptidomimetics I

inferred← citeshttps://doi.org/10.1007/978-3-319-49124-0openalex-snapshot

Peptidomimetics II

inferred← citeshttps://doi.org/10.1007/s00253-019-09957-yopenalex-snapshot

Conversion of phenylglycinonitrile by recombinant Escherichia coli cells synthesizing variants of the arylacetonitrilase from Pseudomonas fluorescens EBC191

inferred← citeshttps://doi.org/10.1007/s00726-013-1539-4openalex-snapshot

Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases; Part 1: alkyl halide alkylations

inferred← citeshttps://doi.org/10.1007/s10562-019-02965-7openalex-snapshot

A New Cobalt(III)/[Mo6O19]2− Heterogeneous Catalyst for Promoting the Oxidative Coupling of Amines to Imines

inferred← citeshttps://doi.org/10.1007/s10562-026-05515-0openalex-snapshot

An Efficient Strecker Synthesis of α-Aminonitriles Under Mild Conditions by ZrO2–SnO2 Solid Acid Catalyst

inferred← citeshttps://doi.org/10.1007/s10800-020-01428-xopenalex-snapshot

Electrosynthesis of glycine from bio-derivable oxalic acid

inferred← citeshttps://doi.org/10.1007/s11030-022-10479-5openalex-snapshot

Natural halloysite nanotubes as an efficient catalyst in strecker reaction: the synthesis of α-amino nitriles under solvent-free conditions

inferred← citeshttps://doi.org/10.1007/s11164-015-2398-2openalex-snapshot

A facile and economic method for the synthesis of (S)-N-Boc-3′-hydroxyadamantylglycine

inferred← citeshttps://doi.org/10.1007/s11164-017-2892-9openalex-snapshot

Brønsted acid-catalyzed aza-Mannich reaction of N-Boc aminals: access to multifunctional rhodanine/hydantoin derivatives

inferred← citeshttps://doi.org/10.1007/s11164-025-05718-xopenalex-snapshot

Zeolite omega-catalyzed synthesis of 2-(phenyl(phenylamino)methyl) malononitrile: spectroscopic analysis, DFT calculations and biological activity prediction

inferred← citeshttps://doi.org/10.1007/s11172-025-4678-3openalex-snapshot

Metal-free organic synthesis in liquefied gases: achievements and prospects

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