Regio- and diastereoselective synthesis of lissoclinolide analogues by Lewis acid catalyzed cyclization of the first 1,5-bis(trimethylsilyloxy)-1,3,5-hexatrienes with oxalyl chloride

Authors
Langer, P Freifeld, I
Citation
P. Langer et I. Freifeld, Regio- and diastereoselective synthesis of lissoclinolide analogues by Lewis acid catalyzed cyclization of the first 1,5-bis(trimethylsilyloxy)-1,3,5-hexatrienes with oxalyl chloride, SYNLETT, (4), 2001, pp. 523-525
Citations number
35
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
SYNLETT
ISSN journal
09365214 → ACNP
Issue
4
Year of publication
2001
Pages
523 - 525
Database
ISI
SICI code
0936-5214(200104):4<523:RADSOL>2.0.ZU;2-D
Abstract
The Lewis acid catalyzed cyclization of 1,5-bis(trimethylsilyloxy)-1,3,5-he xatrienes with oxalyl chloride resulted in formation of polyunsaturated but enolides.