A cascade cyclization approach to schweinfurthin B

Edward M. Treadwell, Jeffrey Neighbors, David F. Wiemer

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

(graph presented) A strategy for synthesis of the hexahydroxanthene moiety of the natural products schweinfurthin A, B, and D is described. The relative stereochemistry in the key cationic cyclization step is established through the preference of the phenylselenide substituent for an equatorial orientation.

Original languageEnglish (US)
Pages (from-to)3639-3642
Number of pages4
JournalOrganic Letters
Volume4
Issue number21
DOIs
StatePublished - Oct 17 2002

All Science Journal Classification (ASJC) codes

  • Molecular Medicine

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