Asymmetric synthesis of enantiomerically pure 4-aminoglutamic acids via methylenedimerization of chiral glycine equivalents with dichloromethane under operationally convenient conditions-Reference-Cited by-同舟云学术

Asymmetric synthesis of enantiomerically pure 4-aminoglutamic acids via methylenedimerization of chiral glycine equivalents with dichloromethane under operationally convenient conditions

Published:2004-12 Issue:50 Volume:45 Page:9159-9162
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Taylor Stephen M.,Yamada Takeshi,Ueki Hisanori,Soloshonok Vadim A.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

1. Biosynthesis of peptidoglycan: points of attack by wall inhibitors

2. Highly Diastereoselective Michael Addition Reactions between Nucleophilic Glycine Equivalents and β-substituted-α,β-Unsaturated Carboxylic acid Derivatives a General Approach to the Stereochemically Defined and Sterically χ-Constrained α-Amino Acids

3. Toward design of a practical methodology for stereocontrolled synthesis of χ-constrained pyroglutamic acids and related compounds. Virtually complete control of simple diastereoselectivity in the Michael addition reactions of glycine Ni(II) complexes with N-(enoyl)oxazolidinones

4. Rational Design of Highly Diastereoselective, Organic Base-Catalyzed, Room-Temperature Michael Addition Reactions1

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