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Issue 40, 2013
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Oxidative ortho-alkenylation of arylphosphine oxides by rhodium-catalyzed C–H bond twofold cleavage

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Abstract

An efficient Rh-catalyed oxidative ortho-alkenylation is reported from the reaction of arylphosphine oxides with activated and non-activated alkenes as well. The developed method is characterized by high selectivity, a wide substrate scope, and an excellent functional group tolerance.

Graphical abstract: Oxidative ortho-alkenylation of arylphosphine oxides by rhodium-catalyzed C–H bond twofold cleavage

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Publication details

The article was received on 27 Jun 2013, accepted on 26 Jul 2013 and first published on 31 Jul 2013


Article type: Communication
DOI: 10.1039/C3RA43764G
Citation: RSC Adv., 2013,3, 18296-18299
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    Oxidative ortho-alkenylation of arylphosphine oxides by rhodium-catalyzed C–H bond twofold cleavage

    J. Mo, S. Lim, S. Park, T. Ryu, S. Kim and P. H. Lee, RSC Adv., 2013, 3, 18296
    DOI: 10.1039/C3RA43764G

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