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Эта публикация цитируется в 8 научных статьях (всего в 8 статьях)
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
Аннотация:
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.
Образец цитирования:
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
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3497 https://www.mathnet.ru/rus/mendc/v16/i1/p15
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