Synthesis of Allocolchicines Using Sequential Ring-Closing Enyne Metathesis−Diels−Alder Reactions-Reference-Cited by-同舟云学术

Synthesis of Allocolchicines Using Sequential Ring-Closing Enyne Metathesis−Diels−Alder Reactions

Published:2007-01-24 Issue:4 Volume:9 Page:715-718
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Boyer François-Didier¹,Hanna Issam¹

Affiliation:

1. Unité de Chimie Biologique, INRA, F-78026 Versailles, France, and Laboratoire de Synthèse Organique associé au CNRS, Ecole Polytechnique, F-91128 Palaiseau, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0630548

Reference17 articles.

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

2. Total Syntheses of Colchicine in Comparison: A Journey through 50 Years of Synthetic Organic Chemistry

3. Synthesis of (S)-(−)-N-acetylcolchinol using intramolecular biaryl oxidative coupling

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

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