Journal of Organic Chemistry p. 10088 - 10101 (2019)
Update date:2022-08-04
Topics:
He, Yimiao
Huang, Lilan
Xie, Limei
Liu, Peng
Wei, Qiongmei
Mao, Fangfang
Zhang, Xuehong
Huang, Jun
Chen, Sijing
Huang, Chusheng
A new and operationally simple approach for palladium-catalyzed C-H functionalization reactions utilizing an organophosphorus/sulfonate hypervalent iodine reagent as both an oxidant and the source of a functional group has been developed. Through this method, the oxidative phosphorylation-, sulfonation-, and hydroxylation of unactivated benzyl C(sp3)-H bonds, along with the hydroxylation and arylation of aryl C(sp2)-H bonds, are successfully realized under mild conditions and with excellent site-selectivity. The versatile C-OSO2R bond provides a platform for a wide array of subsequent diversification reactions.
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