Total synthesis of elaeokanine A

Hans F. Schmitthenner, Steven M. Weinreb

Research output: Contribution to journalArticle

42 Citations (Scopus)

Abstract

A new general approach to synthesis of Elaeocarpus alkaloids is discribed which utilizes the intramolecular imino Diels-Alder reaction as the key ringforming step. The methodology has been applied to total synthesis of the alkaloid Elaeokanine A.

Original languageEnglish (US)
Pages (from-to)3372-3373
Number of pages2
JournalJournal of Organic Chemistry
Volume45
Issue number16
DOIs
StatePublished - Jan 1 1980

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Alkaloids

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

Schmitthenner, H. F., & Weinreb, S. M. (1980). Total synthesis of elaeokanine A. Journal of Organic Chemistry, 45(16), 3372-3373. https://doi.org/10.1021/jo01304a054
Schmitthenner, Hans F. ; Weinreb, Steven M. / Total synthesis of elaeokanine A. In: Journal of Organic Chemistry. 1980 ; Vol. 45, No. 16. pp. 3372-3373.
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Schmitthenner, HF & Weinreb, SM 1980, 'Total synthesis of elaeokanine A', Journal of Organic Chemistry, vol. 45, no. 16, pp. 3372-3373. https://doi.org/10.1021/jo01304a054

Total synthesis of elaeokanine A. / Schmitthenner, Hans F.; Weinreb, Steven M.

In: Journal of Organic Chemistry, Vol. 45, No. 16, 01.01.1980, p. 3372-3373.

Research output: Contribution to journalArticle

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