Efficient asymmetric synthesis of the functionalized pyroglutamate core unit common to oxazolomycin and neooxazolomycin using Michael reaction of nucleophilic glycine Schiff base with α,β-disubstituted acrylate-Reference-Cited by-同舟云学术

Efficient asymmetric synthesis of the functionalized pyroglutamate core unit common to oxazolomycin and neooxazolomycin using Michael reaction of nucleophilic glycine Schiff base with α,β-disubstituted acrylate

Published:2008-12 Issue:24 Volume:19 Page:2789-2795
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Yamada Takeshi,Sakaguchi Kazuhiko,Shinada Tetsuro,Ohfune Yasufumi,Soloshonok Vadim A.

Publisher

Elsevier BV

Subject

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

Reference29 articles.

1. Structure of oxazolomycin, a novel β-lactone antibiotic

2. Novel Bioactive Oxazolomycin Isomers Produced by Streptomyces albus JA3453.

3. Oxazolomycin Esters, Specific Inhibitors of Plant Transformation

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