ChemInform Abstract: Synthesis of the Antitrypanosomal Agent (.+-.)-Hydroxyanthecotulide by Cr(II)-Catalyzed Allylation and Meyer-Schuster Rearrangement

A novel strategy for the stereocontrolled synthesis of anti‐ and syn‐hydroxyanthecotulide is presented.

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Bibliographic Details
Published inChemInform Vol. 43; no. 42; p. no
Main Authors Hodgson, David M., Talbot, Eric P. A., Clark, Barry P.
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 16.10.2012
WILEY‐VCH Verlag
Wiley Subscription Services, Inc
Subjects
diastereoselective syntheses
diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism)
enantioselective syntheses (incl. cis/trans-isomerism)
rearrangements
terpenes
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Summary:A novel strategy for the stereocontrolled synthesis of anti‐ and syn‐hydroxyanthecotulide is presented.
Bibliography:ArticleID:CHIN201242197
istex:AAE130F6682FE3B049185294A2B51FDF2FE5BDEE
ark:/67375/WNG-L0ZJ7CCS-F
ISSN:0931-7597
1522-2667
DOI:10.1002/chin.201242197