1620767-17-0Relevant articles and documents
A NCS mediated oxidative C-H bond functionalization: Direct esterification between a C(sp3)-H bond and carboxylic acids
Zheng, Yang,Mao, Jincheng,Rong, Guangwei,Xu, Xinfang
, p. 8837 - 8840 (2015)
A transition metal free oxidative C-H bond functionalization/esterification of α-alkoxy alkanes with acids is described in this report. This method is effectively mediated by NCS instead of traditional oxidants, like TBHP or its derivatives, and directly
Copper catalyzed C-O bond formation via oxidative cross-coupling reaction of aldehydes and ethers
Wang, Quan,Zheng, Hao,Chai, Wen,Chen, Dianyu,Zeng, Xiaojun,Fu, Renzhong,Yuan, Rongxin
supporting information, p. 6549 - 6553 (2014/08/18)
A practical and efficient construction of C-O bonds via oxidative cross-coupling reaction of aldehydes and ethers has been realized under open air. When 2 mol% copper was used as the catalyst, various α-acyloxy ethers were obtained with up to 93% isolated
Copper-Catalyzed Formation of C-O Bonds by Oxidative Coupling of Benzylic Alcohols with Ethers
Wang, Quan,Geng, Haoran,Chai, Wen,Zeng, Xiaojun,Xu, Min,Zhu, Cheng,Fu, Renzhong,Yuan, Rongxin
, p. 6850 - 6853 (2016/02/19)
The copper-catalyzed formation of C-O bonds by oxidative coupling of benzylic alcohols with ethers was realized in open air. A series of α-acyloxy ethers were obtained in good yields with aqueous tert-butyl hydroperoxide as the oxidant. The copper-catalyzed formation of C-O bonds by oxidative coupling of benzylic alcohols with ethers is realized in open air. A series of α-acyloxy ethers were obtained in good yields with aqueous tert-butyl hydroperoxide as the oxidant.
