INTRAMOLECULAR PALLADIUM-CATALYZED ARYL AMINATION AND ARYL AMIDATION

Authors
WOLFE JP RENNELS RA BUCHWALD SL
Citation
Jp. Wolfe et al., INTRAMOLECULAR PALLADIUM-CATALYZED ARYL AMINATION AND ARYL AMIDATION, Tetrahedron, 52(21), 1996, pp. 7525-7546
Citations number
63
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron → ACNP
ISSN journal
00404020
Volume
52
Issue
21
Year of publication
1996
Pages
7525 - 7546
Database
ISI
SICI code
0040-4020(1996)52:21<7525:IPAAAA>2.0.ZU;2-D
Abstract
Upon treatment with a palladium catalyst and a suitable base, aromatic halides undergo intramolecular substitution to form five, six, and se ven-membered rings. In a similar fashion aryl halides with pendant ami des or sulfonamides are cyclized to form five and six-membered rings. Copyright (C) 1996 Elsevier Science Ltd