Аннотация:
The products of C-vinylation were prepared in 52–65% yield by the reaction of secondary nitroalkanes with acetylene in DMSO– KOH.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
B. F. Kukharev, V. K. Stankevich, G. R. Klimenko, “Nucleophilic addition of secondary nitro compounds to acetylene”, Mendeleev Commun., 12:2 (2002), 63–64
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4093
https://www.mathnet.ru/rus/mendc/v12/i2/p63
Эта публикация цитируется в следующих 3 статьяx:
N. A. Lobanova, I. V. Tatarinova, I. A. Ushakov, E. Yu. Schmidt, B. A. Trofimov, “Reaction of Nitromethane with Phenylacetylene in Superbasic Medium”, Russ J Org Chem, 60:3 (2024), 543
Boris A. Trofimov, Elena Yu. Schmidt, Igor' A. Ushakov, Nadezhda V. Zorina, Elena V. Skital'tseva, Nadezhda I. Protsuk, Al'bina I. Mikhaleva, “Base‐Catalyzed Stereoselective Vinylation of Ketones with Arylacetylenes: A New C(sp3)C(sp2) Bond‐Forming Reaction”, Chemistry A European J, 16:28 (2010), 8516
Boris F. Kukharev, Valery K. Stankevich, Galina R. Klimenko, “Nucleophilic Addition of Secondary Nitro Compounds to Acetylene.”, ChemInform, 33:39 (2002), 59
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