PREPARATION OF ENANTIOMERICALLY ENRICHED ALPHA-ALKOXYSTANNANES BY REGIOSELECTIVE ACETAL EXCHANGE OR ACETAL HYDROLYSIS

Authors
LINDERMAN RJ CUSACK KP JABER MR
Citation
Rj. Linderman et al., PREPARATION OF ENANTIOMERICALLY ENRICHED ALPHA-ALKOXYSTANNANES BY REGIOSELECTIVE ACETAL EXCHANGE OR ACETAL HYDROLYSIS, Tetrahedron letters, 37(37), 1996, pp. 6649-6652
Citations number
29
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
37
Issue
37
Year of publication
1996
Pages
6649 - 6652
Database
ISI
SICI code
0040-4039(1996)37:37<6649:POEEAB>2.0.ZU;2-Q
Abstract
alpha-Alkoxyorganostannanes can be resolved via the methoxymenthyl eth ers with subsequent regioselective acetal exchange or cleavage of the acetal group to the alpha-hydroxyalkylstannane. Copyright (C) 1996 Els evier Science Ltd