Enantioselective total synthesis of the mexicanolides: khayasin, proceranolide, and mexicanolide

Faber, Jonathan M., Eger, Wilhelm A. and Williams, Craig M. (2012) Enantioselective total synthesis of the mexicanolides: khayasin, proceranolide, and mexicanolide. Journal of Organic Chemistry, 77 20: 8913-8921. doi:10.1021/jo301182f


Author Faber, Jonathan M.
Eger, Wilhelm A.
Williams, Craig M.
Title Enantioselective total synthesis of the mexicanolides: khayasin, proceranolide, and mexicanolide
Journal name Journal of Organic Chemistry   Check publisher's open access policy
ISSN 0022-3263
1520-6904
Publication date 2012-01-01
Sub-type Article (original research)
DOI 10.1021/jo301182f
Volume 77
Issue 20
Start page 8913
End page 8921
Total pages 9
Place of publication Washington, DC, United States
Publisher American Chemical Society
Language eng
Abstract The enantioselective total synthesis of the limonoids khayasin, proceranolide and mexicanolide was achieved via a convergent strategy utilizing a tactic aimed at incorporating natural products as advanced intermediates. This extended biomimetically inspired approach additionally achieved the enantioselective total synthesis of the intermediates azedaralide and cipadonoid B.
Q-Index Code C1
Q-Index Status Confirmed Code
Institutional Status UQ

Document type: Journal Article
Sub-type: Article (original research)
Collections: Official 2013 Collection
School of Chemistry and Molecular Biosciences
 
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Created: Fri, 23 Nov 2012, 20:51:20 EST by Mrs Louise Nimwegen on behalf of School of Chemistry & Molecular Biosciences