Stereoselective amination of chiral enolates: Synthesis of enantiomerically pure α,β-diamino acids, chiral key compounds in the synthesis of conformationally constrained peptido- and non-peptidomimetics-Reference-Cited by-同舟云学术

Stereoselective amination of chiral enolates: Synthesis of enantiomerically pure α,β-diamino acids, chiral key compounds in the synthesis of conformationally constrained peptido- and non-peptidomimetics

Published:1995-11 Issue:11 Volume:6 Page:2787-2796
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Badorrey Ramón,Cativiela Carlos,Diaz-de-Villegas Maria D.,Gálvez JoséA.

Publisher

Elsevier BV

Subject

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

Reference23 articles.

1. Chemical studies on tuberactinomycins. X. Total synthesis of tuberactinomycin O

2. Total synthesis of capreomycin

3. Syntheses of Capreomycin Analogs in Relation to Their Antibacterial Activities

4. Total synthesis and absolute stereochemistry of the antifungal dipeptide Sch 37137 and its 2S,3S - isomer

5. Biosynthesis of capreomycin. 2. Incorporation of L-serine, L-alanine, and L-2,3-diaminopropionic acid

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