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Oxidation of Cycloalkenes and Methylenecycloalkanes by Palladium (II) Complexes: Part I. NMR Study on the Mechanism of the Formation of Ring-Contracted and Ring-Opened Products in the Oxidation of 1-Methylcyclobutene Научная публикация

Журнал Journal of Molecular Catalysis
ISSN: 0304-5102
Вых. Данные Год: 1993, Том: 83, Номер: 3, Страницы: 287-300 Страниц : 14 DOI: 10.1016/0304-5102(93)87039-B
Авторы Beck I.E. 1 , Gusevskaya E.V. 1 , Golovin A.V. 1 , Likholobov V.A. 1
Организации
1 Boreskov Institute of Catalysis
Реферат: Oxidation of 1-methylcyclobutene (1) by PdCl2L2 and PdCl(NO2)L2 (LCD3CN) in methylene chloride was studied with 1H and 13C NMR. Reaction of 1 with PdCl2L2 leads to the formation of the stable ring-opened 1-3-η3-π-allyl palladium complex (2). With the addition of an equimolar quantity of PdCl(NO2)L2 to the solution of complex 2, the allylic oxidation of 2 proceeds slowly via the intermediate formation of another 1-3-η3-π-allyl palladium complex (3). When reacting directly with PdCl(NO2)L2, 1 undergoes palladium (II)-catalyzed ring contraction to give cyclopropyl methyl ketone. Kinetic and spectral data indicate the formation of an organometallic intermediate, a product of the β-nitritopalladation of the parent olefin 1.
Библиографическая ссылка: Beck I.E. , Gusevskaya E.V. , Golovin A.V. , Likholobov V.A.
Oxidation of Cycloalkenes and Methylenecycloalkanes by Palladium (II) Complexes: Part I. NMR Study on the Mechanism of the Formation of Ring-Contracted and Ring-Opened Products in the Oxidation of 1-Methylcyclobutene
Journal of Molecular Catalysis. 1993. V.83. N3. P.287-300. DOI: 10.1016/0304-5102(93)87039-B WOS Scopus РИНЦ CAPlusCA OpenAlex Sciact
Даты:
Поступила в редакцию: 10 сент. 1992 г.
Принята к публикации: 20 мар. 1993 г.
Опубликована в печати: 30 июл. 1993 г.
Опубликована online: 2 окт. 2001 г.
Идентификаторы БД:
Web of science: WOS:A1993LQ32700003
Scopus: 2-s2.0-0027627787
РИНЦ: 31642027
Chemical Abstracts: 1994:54011
Chemical Abstracts (print): 120:54011
OpenAlex: W1533372520
Sciact: 12866
Цитирование в БД:
БД Цитирований
Scopus 11
OpenAlex 10
Альметрики: