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A stereoselective synthesis of the bromopyrrole natural product (-)-agelastatin A.

ABSTRACT: Weaving an intricate web: A stereoselective synthesis of (-)-agelastatin A has been developed, which requires 11 steps from commercially available starting material. The application of a Rh-catalyzed intramolecular olefin aziridination reaction and the subsequent manipulation of the resulting tricyclic intermediate (see scheme) punctuate this study.

SUBMITTER: Wehn PM

PROVIDER: S-EPMC2791535 | biostudies-literature | 2009

REPOSITORIES: biostudies-literature

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A stereoselective synthesis of the bromopyrrole natural product (-)-agelastatin A.

Wehn Paul M PM Du Bois J J

Angewandte Chemie (International ed. in English) 20090101 21

Weaving an intricate web: A stereoselective synthesis of (-)-agelastatin A has been developed, which requires 11 steps from commercially available starting material. The application of a Rh-catalyzed intramolecular olefin aziridination reaction and the subsequent manipulation of the resulting tricyclic intermediate (see scheme) punctuate this study. ...[more]

PMID: 19378315

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