| Literature DB >> 11674099 |
Anthony G. M. Barrett1, Adrian J. Bennett, Stefan Menzer, Marie L. Smith, Andrew J. P. White, David J. Williams.
Abstract
The total synthesis of restrictinol, the hydrolysis product of the antifungal natural product restricticin, starting from commercially available methyl (S)-(+)-3-hydroxy-2-methylpropionate is described. Key stages in the strategy involved (i) the use of Brown's allylboration chemistry to construct an acyclic intermediate bearing three of the four stereogenic centers of the natural product, (ii) formation of a C-glycosidic vinyl iodide, and (iii) introduction of the triene side chain via a Suzuki coupling reaction.Entities:
Year: 1999 PMID: 11674099 DOI: 10.1021/jo9815305
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354