Literature DB >> 27167881

Copper-Catalyzed Carbonylative Coupling of Cycloalkanes and Amides.

Yahui Li1, Kaiwu Dong1, Fengxiang Zhu1, Zechao Wang1, Xiao-Feng Wu2,3.   

Abstract

Carbonylation reactions are a most powerful method for the synthesis of carbonyl-containing compounds. However, most known carbonylation procedures still require noble-metal catalysts and the use of activated compounds and good nucleophiles as substrates. Herein, we developed a copper-catalyzed carbonylative transformation of cycloalkanes and amides. Imides were prepared in good yields by carbonylation of a C(sp(3) )-H bond of the cycloalkane with the amides acting as weak nucleophiles. Notably, this is the first report of copper-catalyzed carbonylative C-H activation.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  amides; carbonylation; copper catalysis; cycloalkanes; imides

Year:  2016        PMID: 27167881     DOI: 10.1002/anie.201603235

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

Review 1.  Direct radical functionalization methods to access substituted adamantanes and diamondoids.

Authors:  William K Weigel; Hoang T Dang; Abigail Feceu; David B C Martin
Journal:  Org Biomol Chem       Date:  2021-12-22       Impact factor: 3.890

2.  Metal-free photoredox-catalyzed direct α-oxygenation of N,N-dibenzylanilines to imides under visible light.

Authors:  Nalladhambi Neerathilingam; Ramasamy Anandhan
Journal:  RSC Adv       Date:  2022-03-15       Impact factor: 3.361

  2 in total

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