Asymmetric synthesis of the diastereoisomers of L-1-indanylglycine and L-1-benz[f]indanylglycine, χ1,χ2-constrained side-chain derivatives of L-phenylalanine and L-2-naphthylalanine-Reference-Cited by-同舟云学术

Asymmetric synthesis of the diastereoisomers of L-1-indanylglycine and L-1-benz[f]indanylglycine, χ1,χ2-constrained side-chain derivatives of L-phenylalanine and L-2-naphthylalanine

Published:1992-11 Issue:11 Volume:3 Page:1351-1354
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Josien Hubert,Chassaing Gérard

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference11 articles.

1. SYNTHESIS OF AMINO ACIDS FROM SUBSTITUTED CYANOACETIC ESTERS

2. Asymmetric induction at C(β) and C(α) of N-enoyl sultams by 1,4-hydride addition/enolate trapping

3. Asymmetric synthesis of α-amino acids and α-N-hydroxyamino acids via electrophilic amination of bornanesultam-derived enolates with 1-chloro-1-nitrosocyclohexane.

4. Asymmetric alkylations of a sultam-derived glycinate equivalent: practical preparation of enantiomerically pure α-amino acids

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