Abstract
Two synthetic approaches of simpler jaspamide derivatives were investigated. The ring closure step was attempted either by RCM or by macrolactonisation. 14-Membered ring derivatives 15-16 were prepared by final macrolactonisation using Yamaguchi reagent.
Keywords: alkaloid, macrocycle, olefin metathesis, macrolactonisation
Letters in Organic Chemistry
Title: Synthesis of 14-Membered Ring Jaspamide Derivatives
Volume: 2 Issue: 6
Author(s): S. Celanire, C. Descamps-Francois, B. Lesur, G. Guillaumet and B. Joseph
Affiliation:
Keywords: alkaloid, macrocycle, olefin metathesis, macrolactonisation
Abstract: Two synthetic approaches of simpler jaspamide derivatives were investigated. The ring closure step was attempted either by RCM or by macrolactonisation. 14-Membered ring derivatives 15-16 were prepared by final macrolactonisation using Yamaguchi reagent.
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Cite this article as:
Celanire S., Descamps-Francois C., Lesur B., Guillaumet G. and Joseph B., Synthesis of 14-Membered Ring Jaspamide Derivatives, Letters in Organic Chemistry 2005; 2 (6) . https://dx.doi.org/10.2174/1570178054640697
DOI https://dx.doi.org/10.2174/1570178054640697 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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