aJiangsu Police Institute, Nanjing, P.R. China bNanjing Institute of Technology, Nanjing, P.R. China cCollege of Pharmaceutics, Jinhua Polytechnic, Jinhua, P.R. China
Abstract:
A simple rhodium-catalyzed addition reaction of aldehydes with arylboronic acids in aqueous γ-valerolactone provides the corresponding benzylic alcohols in moderate to good yields. Other organoboron reagents (boronic esters, aryl-trifluoroborates, etc.) also showed good compatibilities, albeit with relatively lower yields.
Citation:
M.-x. Xu, K.-M. Zhang, J. Zhang, “A simple rhodium-catalyzed addition reaction of aldehydes with arylboronic acids in aqueous γ-valerolactone”, Mendeleev Commun., 32:3 (2022), 397–398
Linking options:
https://www.mathnet.ru/eng/mendc677
https://www.mathnet.ru/eng/mendc/v32/i3/p397
This publication is cited in the following 2 articles:
A. A. Kurokhtina, E. V. Larina, N. A. Lagoda, A. F. Schmidt, “Active Pd species in the formation of polysubstituted olefins and naphthalenes in the reaction between arylboronic acid and diphenylacetylene”, Mendeleev Commun., 34:2 (2024), 215–217
Naoki Arai, Yuga Shibuya, Shinichi Koguchi, Tetsuya Yamamoto, “Halogen‐Substituted Mesoionic‐Carbene/Palladium Complexes for Catalytic Arylation of Aldehydes”, Asian J Org Chem, 12:5 (2023)
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