Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5283380 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
A variety of benzyl halides were converted to the corresponding aldehydes/ketones in respectable yields by IBX in DMSO at 65 °C. The bromohydrin reaction of olefins using NBS-H2O in DMSO can be nicely adapted to IBX-mediated oxidation of benzyl halides in such a way that olefins are converted to the corresponding 1,2-diketones in good isolated yields in one-pot.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jarugu Narasimha Moorthy, Nidhi Singhal, Kalyan Senapati,