Pd-catalyzed aminocarbonylation of alkynes with amines using Co2(CO)8 as a carbonyl source

文献情報

出版日 2016-03-28

DOI 10.1039/C6QO00075D

インパクトファクター 5.281

著者

Yaxi Dong, Suyan Sun, Fan Yang, Yu Zhu, Weiguo Zhu, Huijie Qiao, Yangjie Wu

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要旨

A simple and mild protocol for the synthesis of 2-ynamides by palladium-catalyzed aminocarbonylation of alkynes was developed. The reaction proceeded at room temperature in air, utilizing Co2(CO)8 as a carbonyl source. This aminocarbonylation reaction features mild reaction conditions and good tolerance of substrates especially including aryl amines and primary amines.

掲載誌

Organic Chemistry Frontiers

CiteScore: 7.8

自己引用率: 8.7%

年間論文数: 724

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

Pd-catalyzed aminocarbonylation of alkynes with amines using Co2(CO)8 as a carbonyl source

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