N-(trans-1-Propenyl)carbazole: an excellent dienophile for cation radical Diels-Alder cycloadditions

Authors
Gao, DX Bauld, NL
Citation
Dx. Gao et Nl. Bauld, N-(trans-1-Propenyl)carbazole: an excellent dienophile for cation radical Diels-Alder cycloadditions, TETRAHEDR L, 41(32), 2000, pp. 5997-6000
Citations number
7
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
41
Issue
32
Year of publication
2000
Pages
5997 - 6000
Database
ISI
SICI code
0040-4039(20000805)41:32<5997:NAEDFC>2.0.ZU;2-A
Abstract
The efficient, regiospecific, and periselective Diels-Alder cycloadditions of N-(trans-1-propenyl)carbazole, a highly electron rich dienophile, to bot h acyclic and cyclic conjugated dienes is found to be induced by tris(4-bro mophenyl)aminium hexachloroantimonate. (C) 2000 Elsevier Science Ltd. All r ights reserved.