Regio- and diastereoselective synthesis of functionalized cyclopentenones by domino Michael-Ester-Wittig reactions of (3-alkoxycarbonyl-2-oxopropylidene)triphenylphosphoranes with maleic diesters

Authors
Langer, P Kracke, B
Citation
P. Langer et B. Kracke, Regio- and diastereoselective synthesis of functionalized cyclopentenones by domino Michael-Ester-Wittig reactions of (3-alkoxycarbonyl-2-oxopropylidene)triphenylphosphoranes with maleic diesters, SYNLETT, (11), 2001, pp. 1790-1792
Citations number
17
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
SYNLETT
ISSN journal
09365214 → ACNP
Issue
11
Year of publication
2001
Pages
1790 - 1792
Database
ISI
SICI code
0936-5214(200111):11<1790:RADSOF>2.0.ZU;2-E
Abstract
The domino Michael-Ester-Wittig reaction of maleic diesters with (3-alkoxyc arbonyl-2-oxopropylidene)triphenylphosphoranes resulted in regio- and diast ereoselective formation of functionalized cyclopentenones.