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Method of preparation of alkylated 1,3-diphenylpropan-2-ones, the components for assembly of graphene nanostructures Full article

Journal Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171
Output data Year: 2020, Volume: 69, Number: 1, Pages: 172-175 Pages count : 4 DOI: 10.1007/s11172-020-2740-8
Tags Grignard reagents; cross-coupling reactions; alkylation; long-chain 1; 3-dialkyl-phenyl-2-propanones
Authors Ten Yu.A. 1 , Troshkova N.M. 1 , Tretyakov E.V. 1,2
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, 9 Akad Lavrentieva Prosp, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, 2 Ul Pirogova, Novosibirsk 630090, Russia

Abstract: Long-chain alkylated 1,3-diphenyl-2-propanones are used in the synthesis of graphene nanostructures (graphene nanoribbons and quantum dots). A reliable procedure to obtain mono- or dialkylated diphenyl-2-propanones in 26 and 38% yields has been proposed. The method includes the dioxolane protection of the keto group in 1,3-di-(4-bromophenyl)-2-propanone, then a palladium-catalyzed cross-coupling reaction of the obtained dioxolane with one-and-a-half- or four-fold excess of dodecyl magnesium bromide that leads to a predominant formation of mono- or dialkylation products respectively, followed by hydrolysis of dioxolanes at the last stage to form the desired diphenyl-2-propanones.
Cite: Ten Y.A. , Troshkova N.M. , Tretyakov E.V.
Method of preparation of alkylated 1,3-diphenylpropan-2-ones, the components for assembly of graphene nanostructures
Russian Chemical Bulletin. 2020. V.69. N1. P.172-175. DOI: 10.1007/s11172-020-2740-8 WOS Scopus РИНЦ OpenAlex
Original: Тен Ю.А. , Трошкова Н.М. , Третьяков Е.В.
МЕТОД ПОЛУЧЕНИЯ АЛКИЛИРОВАННЫХ 1,3-ДИФЕНИЛПРОПАН-2-ОНОВ - КОМПОНЕНТОВ СБОРКИ ГРАФЕНОВЫХ НАНОСТРУКТУР
Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2020. №1. С.172-175. РИНЦ
Dates:
Published print: Jan 1, 2020
Published online: Apr 8, 2020
Identifiers:
Web of science: WOS:000524864100023
Scopus: 2-s2.0-85083320664
Elibrary: 43293035
OpenAlex: W3015679466
Citing:
DB Citing
Web of science 3
Scopus 3
Elibrary 3
OpenAlex 3
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