4.7 Article

Oxidative Aminocarbonylation of Terminal Alkynes for the Synthesis of Alk-2-ynamides by Using Palladium-on-Carbon as Efficient, Heterogeneous, Phosphine-Free, and Reusable Catalyst

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ADVANCED SYNTHESIS & CATALYSIS
卷 354, 期 10, 页码 2049-2056

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201200041

关键词

alk-2-ynamides; heterogeneous catalysis; oxidative aminocarbonylation; palladium-on-carbon (Pd; C); phosphine-free conditions

资金

  1. CSIR (Council of Scientific and Industrial Research) New Delhi, India

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Palladium-on-carbon (Pd/C)-catalyzed oxidative aminocarbonylations of alk-1-ynes with secondary amines provide the corresponding alk-2-ynamides in a good to excellent yields. This new methodology is applicable for the synthesis of a wide range of biologically active alk-2-ynamide derivatives. The developed protocol avoids the use of phosphine ligands, with an additional advantage of palladium catalyst recovery and reuse for up to four consecutive cycles.

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