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Palladium-catalyzed intermolecular carbonylative cross-coupling of heteroaryl C(sp 2 )-H bonds with amines: an efficient strategy for oxidative aminocarbonylation of azoles
An efficient palladium-catalyzed oxidative aminocarbonylation of azoles has been developed. This system allows for intermolecular carbonylative cross-coupling of aromatic C(sp )-H bonds with simple amines, which has often been asked for, but has not been realized so far. It provides a straightforwar...
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Published in: | Chemical communications (Cambridge, England) England), 2017, Vol.53 (51), p.6914-6917 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | An efficient palladium-catalyzed oxidative aminocarbonylation of azoles has been developed. This system allows for intermolecular carbonylative cross-coupling of aromatic C(sp
)-H bonds with simple amines, which has often been asked for, but has not been realized so far. It provides a straightforward approach to a variety of azol-2-amides. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c7cc03274a |