1284251-41-7Relevant articles and documents
Synthesis of α-acyloxy ethers via direct esterification of carboxylic acids with ethers under metal-organic framework catalysis
Ha, Phuong T.M.,Le, Thuan D.,Doan, Son H.,Nguyen, Tung T.,Le, Nhan T.H.,Phan, Nam T.S.
, p. 5883 - 5891 (2017)
An iron-organic framework MOF-235 was synthesized, and utilized as an effective heterogeneous catalyst for the synthesis of α-acyloxy ethers via direct esterification of carboxylic acids with C(sp3)[sbnd]H bonds. The iron-based framework showed
Copper corrole catalyzed esterification of C(sp3)-H with carboxylic acids via cross-dehydrogenative coupling reaction
Liu, Zhao-Yang,Peng, Wei-Yu,Akram, Waseem,Lai, Jia-Wei,Zhang, Hao,Liu, Hai-Yang
, p. 860 - 870 (2021/05/19)
Copper corrole complex was firstly used as catalyst for oxidative esterification of un-reactive C(sp3)-H bond of cyclic ether and carboxylic acid via cross-dehydrogenative coupling (CDC) reaction using di-tert-butyl peroxide (DTBP) as oxidant.
Iron porphyrin-catalyzed C(SP3) -H activation for the formation of C–O bond via cross-dehydrogenative coupling of cycloether and aromatic acid
Wen, Wei-Hong,Xie, An-Na,Wang, Hua-Hua,Zhang, Dong-Xu,Ali, Atif,Ying, Xiao,Liu, Hai-Yang
, p. 7169 - 7176 (2017/11/17)
An efficient cyclic ether benzoxylation was achieved by using iron porphyrin as the catalyst and di-tert-butyl peroxide oxidant. The benzoic acid substrates bearing electron donating or withdrawing groups could react with cyclic ether smoothly to afford t
