Indium trihalide mediated regioselective ring opening of aziridines: A facile synthesis of 2-haloamines

Authors
Yadav, JS Reddy, BVS Kumar, GM
Citation
Js. Yadav et al., Indium trihalide mediated regioselective ring opening of aziridines: A facile synthesis of 2-haloamines, SYNLETT, (9), 2001, pp. 1417-1418
Citations number
16
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
SYNLETT
ISSN journal
09365214 → ACNP
Issue
9
Year of publication
2001
Pages
1417 - 1418
Database
ISI
SICI code
0936-5214(200109):9<1417:ITMRRO>2.0.ZU;2-I
Abstract
A variety of N-tosyl aziridines undergo ring opening with indium trihalides in acetonitrile at ambient temperature to afford the corresponding haloami nes in excellent yields with high regioselectivity.