| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5268080 | Tetrahedron Letters | 2012 | 5 Pages |
Abstract
An efficient protocol for the synthesis of vicinal bromohydrins and dibromides from olefins is presented. Various olefins are regio- and stereoselectively hydroxybrominated and dibrominated with anti fashion, following Markonikov's rule, using eco-friendly, non-toxic, and stable reagents such as NH4Br and oxone® in CH3CN/H2O (1:1) and CH3CN without employing catalyst in moderate to excellent yields. Bromohydrins are formed instantaneously.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Arun Kumar Macharla, Rohitha Chozhiyath Nappunni, Narender Nama,