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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2021, том 31, выпуск 2, страницы 271–273 (Mi mendc903)

Эта публикация цитируется в 3 статьях

Communications

Nickel catalyzed hydrosilane reduction of (het)arenecarboxylic acids into aldehydes

L. Wanga, Ya. Wangb, Yu. Taoa, N. Zhanga, Sh. Lia

a School of Chemical and Pharmaceutical Engineering, Changzhou Vocational Institute of Engineering, Changzhou, P.R. China
b School of Petrochemical Engineering, Changzhou University, Changzhou, China


Аннотация: Nickel-catalyzed reduction of (het)arenecarboxylic acids with hydrosilanes in the presence of dimethyl dicarbonate as the activator affords the corresponding aldehydes. The role of the activator is the conversion of the acids into their anhydrides undergoing C–O cleavage. The good yields were achieved in case of substrates bearing electron-donating and electron-neutral groups.

Ключевые слова: nickel catalysis, C–O cleavage, arenecarboxylic acids, aldehydes, hydrosilanes, dimethyl dicarbonate.

Язык публикации: английский

DOI: 10.1016/j.mencom.2021.03.043



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