Jump to main content
Jump to site search

Issue 27, 2014
Previous Article Next Article

Copper-catalyzed tandem oxidative cyclization of cinnamamides with benzyl hydrocarbons through cross-dehydrogenative coupling

Author affiliations

Abstract

The copper-catalyzed tandem oxidative cyclization of cinnamamides with benzyl hydrocarbons through the direct cross-dehydrogenative coupling of sp3 and sp2 C–H bonds has been developed. Satisfactorily, ethers, alcohols and alkanes could also be used instead of benzyl hydrocarbons in this transformation, which allows rapid access to diverse dihydroquinolinones in one step.

Graphical abstract: Copper-catalyzed tandem oxidative cyclization of cinnamamides with benzyl hydrocarbons through cross-dehydrogenative coupling

Back to tab navigation

Supplementary files

Publication details

The article was received on 24 Jan 2014, accepted on 11 Feb 2014 and first published on 12 Feb 2014


Article type: Communication
DOI: 10.1039/C4CC00637B
Chem. Commun., 2014,50, 3589-3591

  •   Request permissions

    Copper-catalyzed tandem oxidative cyclization of cinnamamides with benzyl hydrocarbons through cross-dehydrogenative coupling

    S. Zhou, L. Guo, S. Wang and X. Duan, Chem. Commun., 2014, 50, 3589
    DOI: 10.1039/C4CC00637B

Search articles by author

Spotlight

Advertisements