Indium tribromide catalyzed highly regioselective ring opening of epoxides and aziridines with pyrrole

Yadav, J. S. ; Reddy, B. V. S. ; Parimala, G. (2002) Indium tribromide catalyzed highly regioselective ring opening of epoxides and aziridines with pyrrole Synlett, 2002 (7). pp. 1143-1145. ISSN 0936-5214

Full text not available from this repository.

Official URL: http://www.thieme-connect.com/ejournals/abstract/s...

Related URL: http://dx.doi.org/10.1055/s-2002-32575

Abstract

Pyrrole reacts smoothly with terminal epoxides in the presence of a catalytic amount of InBr3 under very mild conditions to afford the corresponding C-alkylated pyrroles in high yields. Similarly, activated aziridines also opened by pyrrole under the influence of indium tribromide to afford 2- and 3-alkyl pyrrole derivatives in high yields with high regioselectivity.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:Indium Reagents; Epoxides; C-alkylation; Pyrrole
ID Code:62794
Deposited On:24 Sep 2011 04:41
Last Modified:24 Sep 2011 04:41

Repository Staff Only: item control page