Stereoselective Construction of the Complete Ingenane Ring System

Raymond Lee Funk, Thomas A. Olmstead, M. Parvez, John B. Stallman

Research output: Contribution to journalArticle

41 Citations (Scopus)

Abstract

A stereoselective route to the fully assembled and optically pure tetracyclic ring system of ingenol which features a macrocyclic Claisen rearrangement for the construction of the strained in,out-bridged bicyclic substructure and simultaneous, strategic placement of functionality has been developed.

Original languageEnglish (US)
Pages (from-to)5873-5875
Number of pages3
JournalJournal of Organic Chemistry
Volume58
Issue number22
DOIs
StatePublished - Jan 1 1993

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ingenane
ingenol

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

Funk, Raymond Lee ; Olmstead, Thomas A. ; Parvez, M. ; Stallman, John B. / Stereoselective Construction of the Complete Ingenane Ring System. In: Journal of Organic Chemistry. 1993 ; Vol. 58, No. 22. pp. 5873-5875.
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Stereoselective Construction of the Complete Ingenane Ring System. / Funk, Raymond Lee; Olmstead, Thomas A.; Parvez, M.; Stallman, John B.

In: Journal of Organic Chemistry, Vol. 58, No. 22, 01.01.1993, p. 5873-5875.

Research output: Contribution to journalArticle

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