Iron porphyrin-catalyzed C(SP3) -H activation for the formation of CO bond via cross-dehydrogenative coupling of cycloether and aromatic acid
-
Add time:07/18/2019 Source:sciencedirect.com
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 the desired products. It was found iron porphyrin catalyzed oxidative C (sp3)-H activating esterification had the advantage of short reaction time and low catalyst loading. The reaction had been proved to proceed via a radical process.
We also recommend Trading Suppliers and Manufacturers of 4-chloro-1-naphthalenecarboxylic acid (cas 1013-04-3). Pls Click Website Link as below: cas 1013-04-3 suppliers
Prev:Synthesis of 4-hydroxy- and 2,4-dihydroxy-homophthalates by [4+2] cycloaddition of 1,3-bis(silyloxy)-1,3-butadienes with dimethyl allene-1,3-dicarboxylate
Next:1-Benzyl-2-methyl-3-indolylmethylene barbituric acid derivatives: Anti-cancer agents that target nucleophosmin 1 (NPM1)) - 【Back】【Close 】【Print】【Add to favorite 】
-
Health and Chemical more >


