Article ID Journal Published Year Pages File Type
5271701 Tetrahedron Letters 2013 4 Pages PDF
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
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