DISPIROKETALS IN SYNTHESIS .13. FUNCTIONALIZED DISPIROKETALS AS NEW CHIRAL AUXILIARIES - HIGHLY STEREOSELECTIVE DIELS-ALDER REACTIONS USINGA BIFUNCTIONAL, C-2-SYMMETRICAL CHIRAL AUXILIARY

Authors
BEZUIDENHOUDT BCB CASTLE GH GEDEN JV LEY SV
Citation
Bcb. Bezuidenhoudt et al., DISPIROKETALS IN SYNTHESIS .13. FUNCTIONALIZED DISPIROKETALS AS NEW CHIRAL AUXILIARIES - HIGHLY STEREOSELECTIVE DIELS-ALDER REACTIONS USINGA BIFUNCTIONAL, C-2-SYMMETRICAL CHIRAL AUXILIARY, Tetrahedron letters, 35(40), 1994, pp. 7451-7454
Citations number
3
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
35
Issue
40
Year of publication
1994
Pages
7451 - 7454
Database
ISI
SICI code
0040-4039(1994)35:40<7451:DIS.FD>2.0.ZU;2-Y
Abstract
Highly selective, asymmetric, Lewis acid catalysed Diels-Alder reactio ns are reported with a bifunctional, C-2-symmetrical diacrylate deriva tive obtained from a chiral auxiliary based on dihydroxylated dispirok etals.