About: A Chemoenzymatic Total Synthesis of ent-Bengamide E

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Attributs	Valeurs
type	work Article
Is Part Of	http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_20/w
Subject	Article
Title	A Chemoenzymatic Total Synthesis of ent-Bengamide E
has manifestation of work	http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_20/101021jo0159486/m/print http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_20/101021jo0159486/m/web
related by	http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_20/101021jo0159486/authorship/2 http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_20/101021jo0159486/authorship/1
Author	Banwell Martin G. McRae Kenneth J.
Abstract	The cis-1,2-dihydrocatechol 3, which can be obtained in enantiomerically pure form by microbialdihydroxylation of bromobenzene, has been converted into the enantiomer, ent-1, of the cyclolysine-based marine natural product bengamide E (1).
article type	research-article
is part of this journal	The Journal of Organic Chemistry

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