| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5229562 | Tetrahedron | 2007 | 10 Pages |
Abstract
The atom-efficient cross-coupling reaction of triarylbismuths with a variety of aliphatic, aromatic, and hetero-aromatic acyl chlorides was demonstrated to afford high yields of cross-coupled ketones under palladium catalysis. The corresponding cross-coupling reaction with diacid chlorides also furnished bis-coupled ketones in good yields.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Maddali L.N. Rao, Varadhachari Venkatesh, Debasis Banerjee,