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This article is cited in 8 scientific papers (total in 8 papers)
Stereoselective formation of a 3,5-trans-disubstituted 1,4-tetramethylene-(tetrahydro-2,2-furylidene)ammonium salt in bromination of 2-phenylthiopent-4-enoic acid dialkylamide
A. V. Lozanova, T. M. Ugurchieva, M. V. Zlokazov, A. V. Stepanov, V. V. Veselovsky
N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract:
The reaction of N-(2-phenylthiopent-4-enoyl)pyrrolidine with bromine results in the stereoselective formation of 1,4-tetramethylene(5S*-bromomethyl-3R*-phenylthiotetrahydro-2,2-furylidene)ammonium bromide.
Citation:
A. V. Lozanova, T. M. Ugurchieva, M. V. Zlokazov, A. V. Stepanov, V. V. Veselovsky, “Stereoselective formation of a 3,5-trans-disubstituted 1,4-tetramethylene-(tetrahydro-2,2-furylidene)ammonium salt in bromination of 2-phenylthiopent-4-enoic acid dialkylamide”, Mendeleev Commun., 16:1 (2006), 15–16
Linking options:
https://www.mathnet.ru/eng/mendc3497 https://www.mathnet.ru/eng/mendc/v16/i1/p15
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