DIASTEREOSELECTIVE [3-PHENLTHIOCYCLOPROPYL KETONE WITH ENOL SILYL ETHERS - SYNTHESIS OF FUNCTIONALIZED CYCLOPENTANES(2] CYCLOADDITION OF METHYL 2)

Authors
HORIGUCHI Y SUEHIRO I SASAKI A KUWAJIMA I
Citation
Y. Horiguchi et al., DIASTEREOSELECTIVE [3-PHENLTHIOCYCLOPROPYL KETONE WITH ENOL SILYL ETHERS - SYNTHESIS OF FUNCTIONALIZED CYCLOPENTANES(2] CYCLOADDITION OF METHYL 2), Tetrahedron letters, 34(38), 1993, pp. 6077-6080
Citations number
13
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
34
Issue
38
Year of publication
1993
Pages
6077 - 6080
Database
ISI
SICI code
0040-4039(1993)34:38<6077:D[KWES>2.0.ZU;2-3
Abstract
Dimethylaluminum chloride-mediated [3 + 2] cycloaddition of methyl 2-p henylthiocyclopropyl ketone and enol TBDPS or TIPS ethers proceeds hig hly diastereoselectively to afford functionalized cyclopentanes in goo d yields.