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
Collection year 2013
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
 
Versions
Version Filter Type
Citation counts: TR Web of Science Citation Count  Cited 12 times in Thomson Reuters Web of Science Article | Citations
Scopus Citation Count Cited 12 times in Scopus Article | Citations
Google Scholar Search Google Scholar
Created: Fri, 23 Nov 2012, 20:51:20 EST by Mrs Louise Nimwegen on behalf of School of Chemistry & Molecular Biosciences