Diels−Alder Reaction−Aromatization Approach toward Functionalized Ring C Allocolchicinoids. Enantioselective Total Synthesis of (−)-7S-Allocolchicine-Reference-Cited by-同舟云学术

Diels−Alder Reaction−Aromatization Approach toward Functionalized Ring C Allocolchicinoids. Enantioselective Total Synthesis of (−)-7S-Allocolchicine

Published:2003-06-28 Issue:15 Volume:68 Page:5826-5831
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Vorogushin Andrei V.¹,Predeus Alexander V.¹,Wulff William D.¹,Hansen Hans-Jürgen¹

Affiliation:

1. Department of Chemistry, Michigan State University, East Lansing, Michigan 48824, and Institute of Organic Chemistry, University of Zürich, Winterthurerstrasse 190, CH-8057, Zürich, Switzerland

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo034420t

Reference35 articles.

1. (b) Boye, O.; Brossi, A. InThe Alkaloids; Brossi, A., Cordell, G. A., Eds.; Academic Press: New York, 1992; Vol. 41, p 125 and references therein.

2. Bioactive alkaloids. 4. Results of recent investigations with colchicine and physostigmine

3. Antitumor Agents. Part 184. Syntheses and antitubulin activity of compounds derived from reaction of thiocolchicone with amines: Lactams, alcohols, and ester analogs of allothiocolchicinoids

4. Antitumor Agents. 183. Syntheses, Conformational Analyses, and Antitubulin Activity of Allothiocolchicinoids

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