Preparation and catalytic enantioselective reactions of C-3-symmetric tris(oxazoline)s derived from Kemp's triacid

Citation
Th. Chuang et al., Preparation and catalytic enantioselective reactions of C-3-symmetric tris(oxazoline)s derived from Kemp's triacid, SYN COMMUN, 30(9), 2000, pp. 1627-1641
Citations number
93
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
SYNTHETIC COMMUNICATIONS
ISSN journal
00397911 → ACNP
Volume
30
Issue
9
Year of publication
2000
Pages
1627 - 1641
Database
ISI
SICI code
0039-7911(2000)30:9<1627:PACERO>2.0.ZU;2-0
Abstract
Kemp's triacid was elaborated to optically pure tris(beta-hydroxylamide)s a nd tris(oxazoline)s. The resulting C-3-symmetric compounds were used in die thylzinc additions to benzaldehyde and allylic oxidations of cyclopentene, based on Kharash reaction conditions, to give the corresponding products in good chemical yields and moderate enantioselectivities.