A cascade cyclization approach to schweinfurthin B

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

Research output: Contribution to journalArticle

25 Citations (Scopus)

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

Fingerprint

Stereochemistry
Cyclization
stereochemistry
Biological Products
cascades
synthesis
products
schweinfurthin B
schweinfurthin A

All Science Journal Classification (ASJC) codes

  • Molecular Medicine

Cite this

Treadwell, Edward M. ; Neighbors, Jeffrey ; Wiemer, David F. / A cascade cyclization approach to schweinfurthin B. In: Organic Letters. 2002 ; Vol. 4, No. 21. pp. 3639-3642.
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A cascade cyclization approach to schweinfurthin B. / Treadwell, Edward M.; Neighbors, Jeffrey; Wiemer, David F.

In: Organic Letters, Vol. 4, No. 21, 17.10.2002, p. 3639-3642.

Research output: Contribution to journalArticle

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AU - Wiemer, David F.

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