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Issue 23, 2012
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A novel C-5′ substituted cinchona alkaloid-derived catalyst promotes additions of alkyl thiols to nitroolefins with excellent enantioselectivity

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Abstract

A new bifunctional C-5′ substituted cinchona alkaloid-based catalyst promotes the first highly enantioselective additions of alkyl thiols to nitrostyrenes.

Graphical abstract: A novel C-5′ substituted cinchona alkaloid-derived catalyst promotes additions of alkyl thiols to nitroolefins with excellent enantioselectivity

  • This article is part of the themed collection: Chirality
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Publication details

The article was received on 20 Dec 2011, accepted on 26 Jan 2012 and first published on 10 Feb 2012


Article type: Communication
DOI: 10.1039/C2CC17965B
Citation: Chem. Commun., 2012,48, 2849-2851
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    A novel C-5′ substituted cinchona alkaloid-derived catalyst promotes additions of alkyl thiols to nitroolefins with excellent enantioselectivity

    C. Palacio and S. J. Connon, Chem. Commun., 2012, 48, 2849
    DOI: 10.1039/C2CC17965B

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