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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2021 Volume 31, Issue 2, Pages 271–273 (Mi mendc903)

This article is cited in 3 papers

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

Abstract: 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.

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

Language: English

DOI: 10.1016/j.mencom.2021.03.043



© Steklov Math. Inst. of RAS, 2025