| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278395 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
A one-pot, high yield conversion of carboxylic acids to the corresponding aldehydes and ketones is described. The highlight of this methodology is the in situ generation of Weinreb amides with the Deoxo-Fluor reagent, which undergo nucleophilic reaction with DIBAL-H and Grignard reagents.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Cyrous O. Kangani, David E. Kelley, Billy W. Day,