Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5285396 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
Epoxides and aziridines undergo ring opening efficiently with (bromodimethyl)sulfonium bromide at room temperature to form the corresponding β-bromohydrins and β-bromoamines, respectively. The conversions are highly regioselective and afford the products in excellent yields within a short period of time.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Biswanath Das, Maddeboina Krishnaiah, Katta Venkateswarlu,