Stereoselective synthesis of 2,4-disubstituted butanolides |
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Authors: | A. V. Lozanova T. M. Ugurchieva V. V. Veselovsky |
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Affiliation: | (1) N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991 Moscow, Russian Federation |
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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. |
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Keywords: | substituted butanolides N-(pent-4-enoyl)pyrrolidines electrophilic cyclization substituted (tetrahydrofuran-2-ylidene)ammonium bromides |
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