Synthesis of chiral N-phosphinyl α-imino esters and their application in asymmetric synthesis of α-amino esters by reduction

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Location: Deutsche Nationalbibliothek Frankfurt am Main

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Bibliographic citation: Synthesis of chiral N-phosphinyl α-imino esters and their application in asymmetric synthesis of α-amino esters by reduction ; volume:10 ; pages:653-659
Beilstein journal of organic chemistry ; 10, 653-659

Classification: Chemie

DOI: 10.3762/bjoc.10.57

URN: urn:nbn:de:101:1-2015011510424

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:36 AM CEST

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Synthesis of chiral N-phosphinyl α-imino esters and their application in asymmetric synthesis of α-amino esters by reduction

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Other Objects (12)

Synthesis of N-Unprotected α-Amino Acid Methyl Esters

Catalytic Asymmetric Synthesis of Chiral Allylic Esters

Stereoselective Synthesis of α‐Azido Esters and α‐Amino Acid Derivatives via Matteson Homologation of Boronic Esters

Highly Stereoselective Synthesis of γ,δ‐Unsaturated Quaternary α‐Amino Esters via the Tandem N ‐Alkylation/Claisen Rearrangement of α‐Imino Allylesters

Ni-catalyzed asymmetric hydrogenation of N-aryl imino esters for the efficient synthesis of chiral α-aryl glycines

Molybdenum‐Catalyzed Asymmetric Amination of α‐Hydroxy Esters: Synthesis of α‐Amino Acids

Arylglycine-derivative synthesis via oxidative sp3 C–H functionalization of α-amino esters

Decatungstate‐Photocatalyzed Functionalization of α‐Imino Esters for the Preparation of Unnatural α‐Amino Acid Derivatives

Synthesis of unnatural α-amino esters using ethyl nitroacetate and condensation or cycloaddition reactions

Synthesis of benzyloxycyanophenylboronic esters

Palladium-Catalyzed β-Arylation of α-Amino Esters

One-pot synthesis of enantiomerically pure N-protected allylic amines from N-protected α-amino esters

Synthesis of N-Unprotected α-Amino Acid Methyl Esters

Catalytic Asymmetric Synthesis of Chiral Allylic Esters

Stereoselective Synthesis of α‐Azido Esters and α‐Amino Acid Derivatives via Matteson Homologation of Boronic Esters

Highly Stereoselective Synthesis of γ,δ‐Unsaturated Quaternary α‐Amino Esters via the Tandem N ‐Alkylation/Claisen Rearrangement of α‐Imino Allylesters

Ni-catalyzed asymmetric hydrogenation of N-aryl imino esters for the efficient synthesis of chiral α-aryl glycines

Molybdenum‐Catalyzed Asymmetric Amination of α‐Hydroxy Esters: Synthesis of α‐Amino Acids

Arylglycine-derivative synthesis via oxidative sp3 C–H functionalization of α-amino esters

Decatungstate‐Photocatalyzed Functionalization of α‐Imino Esters for the Preparation of Unnatural α‐Amino Acid Derivatives

Synthesis of unnatural α-amino esters using ethyl nitroacetate and condensation or cycloaddition reactions

Synthesis of benzyloxycyanophenylboronic esters

Palladium-Catalyzed β-Arylation of α-Amino Esters

One-pot synthesis of enantiomerically pure N-protected allylic amines from N-protected α-amino esters

Synthesis of N-Unprotected α-Amino Acid Methyl Esters

Catalytic Asymmetric Synthesis of Chiral Allylic Esters

Stereoselective Synthesis of α‐Azido Esters and α‐Amino Acid Derivatives via Matteson Homologation of Boronic Esters

Highly Stereoselective Synthesis of γ,δ‐Unsaturated Quaternary α‐Amino Esters via the Tandem N ‐Alkylation/Claisen Rearrangement of α‐Imino Allylesters

Ni-catalyzed asymmetric hydrogenation of N-aryl imino esters for the efficient synthesis of chiral α-aryl glycines

Molybdenum‐Catalyzed Asymmetric Amination of α‐Hydroxy Esters: Synthesis of α‐Amino Acids

Arylglycine-derivative synthesis via oxidative sp3 C–H functionalization of α-amino esters

Decatungstate‐Photocatalyzed Functionalization of α‐Imino Esters for the Preparation of Unnatural α‐Amino Acid Derivatives

Synthesis of unnatural α-amino esters using ethyl nitroacetate and condensation or cycloaddition reactions

Synthesis of benzyloxycyanophenylboronic esters

Palladium-Catalyzed β-Arylation of α-Amino Esters

One-pot synthesis of enantiomerically pure N-protected allylic amines from N-protected α-amino esters

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