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Acylative Suzuki coupling of amides: acyl-nitrogen activation via synergy of independently modifiable activating groups†
Xijing Li,Gang Zou
Chemical Communications Pub Date : 02/17/2015 00:00:00 , DOI:10.1039/C5CC00430F
Abstract

A highly efficient palladium-catalyzed acylative cross-coupling of carboxylic amides with arylboronic acids has been achieved via synergistic activation of the Cacyl–N bond by independently modifiable activating groups. Coupling of amides features not only good functional group tolerance but also modifiable reactivities to overcome steric hindrance.

Graphical abstract: Acylative Suzuki coupling of amides: acyl-nitrogen activation via synergy of independently modifiable activating groups
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