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Stereoselective synthesis of 2,4-disubstituted butanolides
Authors:A. V. Lozanova  T. M. Ugurchieva  V. V. Veselovsky
Affiliation:(1) N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991 Moscow, Russian Federation
Abstract:A series of 2,4-disubstituted butanolides was prepared based on the trans-stereoselective electrophilic cyclization of substituted N-(pent-4-enoyl)pyrrolidines. The butanolides may be considered as synthons for this type of natural products. Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 124–129, January, 2007.
Keywords:substituted butanolides   N-(pent-4-enoyl)pyrrolidines  electrophilic cyclization  substituted (tetrahydrofuran-2-ylidene)ammonium bromides
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