IMPROVDED SYNTHESIS OF THE A-E RING SEGMENT OF CIGUATOXIN CTX3C

The improved synthesis of the A-E ring segment of ciguatoxin CTX3C was performed via a highly convergent approach based on intramolecular allylation-RCM methodology.

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Bibliographic Details
Published inHeterocycles Vol. 88; no. 2; pp. 969 - 973
Main Authors Shiroma, Kengo, Asakura, Hiroki, Tanaka, Tokihiro, Takamura, Hiroyoshi, Kadota, Isao
Format Journal Article
LanguageEnglish
Published OXFORD Elsevier 01.01.2014
Subjects
Chemistry
Chemistry, Organic
Physical Sciences
Science & Technology
ACETYLATION
PRACTICAL TOTAL-SYNTHESIS
ALPHA-ACETOXY ETHERS
FRAGMENT
CONVERGENT SYNTHESIS
MARINE TOXINS
CIGUATERA
POLYCYCLIC ETHERS
METATHESIS
RUCL2(=CHR)(PR)
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Summary:The improved synthesis of the A-E ring segment of ciguatoxin CTX3C was performed via a highly convergent approach based on intramolecular allylation-RCM methodology.
ISSN:0385-5414
1881-0942
DOI:10.3987/COM-13-S(S)106