HIGHLY STEREOSELECTIVE ACCESS TO 2,4-SUBSTITUTED AND 2,4,5-SUBSTITUTED TETRAHYDROFURANS FROM ALPHA-SILYLACETIC ESTERS - A STUDY OF HOMOALLYLIC STEREOCONTROL

Authors
ANDREY O LANDAIS Y
Citation
O. Andrey et Y. Landais, HIGHLY STEREOSELECTIVE ACCESS TO 2,4-SUBSTITUTED AND 2,4,5-SUBSTITUTED TETRAHYDROFURANS FROM ALPHA-SILYLACETIC ESTERS - A STUDY OF HOMOALLYLIC STEREOCONTROL, Tetrahedron letters, 34(52), 1993, pp. 8435-8438
Citations number
40
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
34
Issue
52
Year of publication
1993
Pages
8435 - 8438
Database
ISI
SICI code
0040-4039(1993)34:52<8435:HSAT2A>2.0.ZU;2-K
Abstract
Cis-2,4- and cis-cis-2,4,5-substituted tetrahydrofurans have been prep ared stereoselectively using electrophile-mediated cyclization of beta -hydroxyhomoallylsilanes, readily available from alpha-silylacetic est ers.