Functionalized carbocyclic rings via intramolecular Diels-Alder reactions of in situ-generated, gamma substituted, heteroatom-stabilized allyl cations in acidic polar media

Authors
Grieco, PA Kaufman, MD
Citation
Pa. Grieco et Md. Kaufman, Functionalized carbocyclic rings via intramolecular Diels-Alder reactions of in situ-generated, gamma substituted, heteroatom-stabilized allyl cations in acidic polar media, TETRAHEDR L, 40(7), 1999, pp. 1265-1268
Citations number
6
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
40
Issue
7
Year of publication
1999
Pages
1265 - 1268
Database
ISI
SICI code
0040-4039(19990212)40:7<1265:FCRVID>2.0.ZU;2-E
Abstract
The synthesis of highly structured carbocyclic ring systems possessing quat ernary carbon atoms has been realized via intramolecular Diels-Alder reacti ons of in situ-generated, gamma substituted, heteroatom-stabilized allyl ca tions in acidic polar media. (C) 1999 Elsevier Science Ltd. All rights rese rved.