Journal
CATALYSIS SCIENCE & TECHNOLOGY
Volume 5, Issue 10, Pages 4750-4754Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cy00993f
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Funding
- National Natural Science Foundation of China [21373248, 21133011]
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A series of palladium-NHC complexes was prepared and their catalytic activity in the oxidative aminocarbonylation of alkynes with amines has been developed using oxygen as the benign oxidant, leading to an efficient approach toward the formation of a wide range of 2-ynamides with high atom efficiency. Utilizing the distinctive reactivity of this palladium-NHC catalysis, both the aryl and the alkyl of the alkynes could be efficiently incorporated into the 2-ynamide. Mechanistic studies provide some evidence to support that amido-Pd could be transformed into amido-Pd-alkynyl.
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