Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5271701 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
Sonogashira cross-coupling of aryl acetylenes and aroyl chlorides catalyzed by palladium(II) acyclic diaminocarbene complexes was investigated. Reactions were carried out with 0.04 mol % of the catalysts, all of which demonstrated high stability and activity in air. The influence of the reaction conditions (temperature, time, amount of catalyst, solvent) and the structures of the starting compounds on the ratios of cross- (1,3-diarylpropynones) and homo-coupling (1,4-diarylbutadiynes) products was elucidated. The yields of 1,3-diarylpropynones reached 95-98%.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Dmitry S. Ryabukhin, Viktor N. Sorokoumov, Elizaveta A. Savicheva, Vadim P. Boyarskiy, Irina A. Balova, Aleksander V. Vasilyev,