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Issue 39, 2009
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Highly enantioselective intramolecular Michael reactions by D-camphor-derived triazolium salts

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Abstract

Camphor-derived chiral triazolium salts have been found to be highly efficient for asymmetric intramolecular Michael reactions. With 1–5 mol% of the catalyst, the desired products were obtained in excellent yields, with up to 99% ee.

Graphical abstract: Highly enantioselective intramolecular Michael reactions by d-camphor-derived triazolium salts

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Publication details

The article was received on 22 Jul 2009, accepted on 22 Aug 2009 and first published on 08 Sep 2009


Article type: Communication
DOI: 10.1039/B914805A
Citation: Chem. Commun., 2009,0, 5823-5825
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    Highly enantioselective intramolecular Michael reactions by D-camphor-derived triazolium salts

    Y. Li, X. Wang, C. Zheng and S. You, Chem. Commun., 2009, 0, 5823
    DOI: 10.1039/B914805A

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