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The application of (Z)-3-aryl-3-haloenoic acids to the synthesis of (Z)-5-benzylidene-4-arylpyrrol-2(5H)-ones
Authors:Gupton John T  Telang Nakul  Banner Edith J  Kluball Emily J  Hall Kayleigh E  Finzel Kara L  Jia Xin  Bates Spencer R  Welden R Scott  Giglio Benjamin C  Eaton James E  Barelli Peter J  Firich Lauren T  Stafford John A  Coppock Matthew B  Worrall Eric F  Kanters Rene P F  Keertikar Kerry  Osterman Rebecca
Institution:a Department of Chemistry, University of Richmond, Richmond, VA 23173, USA
b Merck Research Labs, 2015 Galloping Hill Road, Kenilworth, NJ 07033, USA
Abstract:Studies directed at the synthesis of (Z)-5-benzylidene-4-arylpyrrol-2(5H)-ones from (Z)-3-aryl-3-haloenoic acids are described. The successful strategy relies on the preparation of (Z)-3-aryl-3-haloenoic acids from acetophenones through the corresponding (Z)-3-aryl-3-haloenals and the conversion of the (Z)-3-aryl-3-haloenoic acids to (Z)-5-benzylidene-4-aryl-5H-furan-2-ones. The furanones were subsequently treated with primary amines and dehydrated to the corresponding (Z)-5-benzylidene-4-arylpyrrol-2(5H)-ones.
Keywords:Haloenals  Haloenoic  acids  Furanones  Pyrrolones
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