Highly substituted cis-β-cyclopentane amino acids: An approach to the synthesis of trehazolin analogues-Reference-Cited by-同舟云学术

Highly substituted cis-β-cyclopentane amino acids: An approach to the synthesis of trehazolin analogues

Published:1993-12 Issue:49 Volume:34 Page:7949-7952
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Elliott Russell P.,Hui Andrew,Fairbanks Antony J.,Nash Robert J.,Winchester Bryan G.,Way Gemma,Smith Colin,Lamont R.Brian,Storer Richard,Fleet George W.J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. A reductive aldol strategy for the synthesis of very highly substituted cyclopentanes from sugar lactones

2. Synthesis of Racemic and Optically Active Cispentacin (FR109615) Using Intramolecular Nitrone-Olefin Cycloaddition.

3. Cispentacin, a new antifungal antibiotic. II. In vitro and in vivo antifungal activities.

4. Synthesis and absolute configuration of trehazolin aminocyclitol moiety

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