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A chemoenzymatic total synthesis of ent-bengamide E

Authors :
Banwell, Martin G.
McRae, Kenneth J.
Source :
Journal of Organic Chemistry. Oct 5, 2001, Vol. 66 Issue 20, p6768, 7 p.
Publication Year :
2001

Abstract

Research has been conducted on the cis-1,2-dihydrocatechol obtained by microbial dihydroxylation of bromobenzene. The conversion of this dihydrocatechol into the enantiomer of the cyclolysine-based marine natural product bengamide E is described.

Subjects

Subjects :
Chemistry, Organic -- Research
Enzymes -- Physiological aspects
Enantiomers -- Physiological aspects
Amides -- Physiological aspects
Benzene -- Physiological aspects
Bromine -- Physiological aspects
Hydroxylation -- Physiological aspects
Biological sciences
Chemistry

Details

ISSN :
00223263
Volume :
66
Issue :
20
Database :
Gale General OneFile
Journal :
Journal of Organic Chemistry
Publication Type :
Academic Journal
Accession number :
edsgcl.80008811

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