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Article
Synthesis of a pentacyclic precursor to the Strychnos alkaloids
The Journal of Organic Chemistry
  • George A. Kraus, Iowa State University
  • P.J. Thomas, Iowa State University
  • Dan Bougie, Iowa State University
  • Li Chen, Iowa State University
Document Type
Article
Publication Version
Published Version
Publication Date
3-1-1990
DOI
10.1021/jo00292a042
Abstract
An advanced intermediate for the synthesis of the Strychnos alkaloids was constructed by a sequence involving an intramolecular Diels-Alder reaction, alkylation of an enol silyl ether, and conversion of the alkylation product into a pentacyclic lactam.
Comments

Reprinted (adapted) with permission from The Journal of Organic Chemistry, 55(5); 1624-1627. Doi: 10.1021/jo00292a042. Copyright 1990 American Chemical Society.

Copyright Owner
American Chemical Society
Language
en
File Format
application/pdf
Citation Information
George A. Kraus, P.J. Thomas, Dan Bougie and Li Chen. "Synthesis of a pentacyclic precursor to the Strychnos alkaloids" The Journal of Organic Chemistry Vol. 55 Iss. 5 (1990) p. 1624 - 1627
Available at: http://works.bepress.com/george_kraus/105/