Aerobic oxidative α-arylation of furans with boronic acids via Pd(II)-catalyzed C–C bond cleavage of primary furfuryl alcohols: sustainable access to arylfurans

Guanghao Huang; Lin Lu; Huanfeng Jiang; Biaolin Yin

doi:10.1039/C7CC07111F

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Aerobic oxidative α-arylation of furans with boronic acids via Pd(ii)-catalyzed C–C bond cleavage of primary furfuryl alcohols: sustainable access to arylfurans†

Guanghao Huang,^a Lin Lu,^a Huanfeng Jiang

^a and Biaolin Yin

*^a

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* Corresponding authors

^a Key Laboratory of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou 510640, P. R. China
E-mail: blyin@scut.edu.cn

Abstract

Aerobic oxidative α-arylation of furans with boronic acids via Pd(II)-catalyzed C–C bond cleavage of primary furfuryl alcohols provides sustainable access to arylfurans. This protocol opens a new avenue for the transformation of readily available furans into other useful compounds.

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Article information

DOI: https://doi.org/10.1039/C7CC07111F
Article type: Communication
Submitted: 12 Sep 2017
Accepted: 18 Oct 2017
First published: 19 Oct 2017

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Chem. Commun., 2017,53, 12217-12220

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Aerobic oxidative α-arylation of furans with boronic acids via Pd(II)-catalyzed C–C bond cleavage of primary furfuryl alcohols: sustainable access to arylfurans

G. Huang, L. Lu, H. Jiang and B. Yin, Chem. Commun., 2017, 53, 12217 DOI: 10.1039/C7CC07111F

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Chemical Communications

Aerobic oxidative α-arylation of furans with boronic acids via Pd(ii)-catalyzed C–C bond cleavage of primary furfuryl alcohols: sustainable access to arylfurans†

Abstract

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Aerobic oxidative α-arylation of furans with boronic acids via Pd(II)-catalyzed C–C bond cleavage of primary furfuryl alcohols: sustainable access to arylfurans

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