Synthesis of enantioenriched 4-thiazolidinone (−)-LY213829 by chemoselective benzylamide cleavage in the presence of a C-S bond-Reference-Cited by-同舟云学术

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Synthesis of enantioenriched 4-thiazolidinone (−)-LY213829 by chemoselective benzylamide cleavage in the presence of a C-S bond

Published:1996-09 Issue:9 Volume:7 Page:2515-2518
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Hansen Marvin M.,Harkness Allen R.,Khau Vien V.,Martinelli Michael J.,Deeter Jack B.

Publisher

Elsevier BV

Subject

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

Reference17 articles.

1. Kinetic resolution of a racemic sulfide by enantioselective sulfoxide formation

2. NAD(P)+-NAD(P)H model. 52. Reduction of olefins by hantzsch ester on silica gel

3. NAD(P)+–NAD(P)H Models. 64. The Quantitative Elucidation of the Mechanistic Aspects in the Silica Gel-Catalyzed Reduction of α,β-Unsaturated Carbonyl Compounds by a Model of NAD(P)H

4. Carbanion-mediated oxidative deprotection of non-enolizable benzylated amides

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