4.2 Article

Boric acid catalyzed thia-Michael reactions in water or alcohols

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JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
卷 269, 期 1-2, 页码 214-217

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ELSEVIER
DOI: 10.1016/j.molcata.2007.01.014

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Michael addition; thiols; alpha,beta-unsaturated olefins; boric acid

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Boric acid acts as an efficient catalyst for the conjugate addition of aliphatic thiols, dithiols and aromatic thiols to alpha,beta-unsaturated nitriles, esters, ketones and aldehydes with very good yields in water at room temperature. The reactions are faster in MeOH or EtOH. The use of boric acid, being a safe chemical, as the catalyst and water as the reaction medium are important attributes in the present protocol. (c) 2007 Elsevier B.V. All rights reserved.

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