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Letter

Total Synthesis of (±)-Isoschizogamine

Supporting Info

Jed L. Hubbs and Clayton H. Heathcock*

Department of Chemistry, University of California, Berkeley, California 94720

Org. Lett., 1999, 1 (8), pp 1315–1317

DOI: 10.1021/ol9902632

Publication Date (Web): September 18, 1999

In papers with more than one author, the asterisk indicates the name of the author to whom inquiries about the paper should be addressed.

, chh@steroid.cchem.berkeley.edu

Abstract

Isoschizogamine has been prepared for the first time. The synthesis requires eight steps from a readily available ketone starting material and features an aminal-forming cyclization that is based on a proposed biosynthetic transformation.

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Published In Issue October 21, 1999
Received September 1, 1999

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Letter

Total Synthesis of (±)-Isoschizogamine

Abstract

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Recommend & Share

Related Content

Explorations on the Asymmetric Total Synthesis of Isoschizogamine

An Approach to the Isoschizozygane Alkaloid Core Using a 1,4-Dipolar Cycloaddition of a Cross-Conjugated Heteroaromatic Betaine

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