化学
邻接
钒
催化作用
氧化裂解
化学选择性
键裂
劈理(地质)
氧气
脱氢
密度泛函理论
光化学
药物化学
有机化学
计算化学
岩土工程
工程类
断裂(地质)
作者
Emanuele Amadio,Joan González‐Fabra,Davide Carraro,William Denis,Blerina Gjoka,Cristiano Zonta,Kristin Bartik,Fabrizio Cavani,Stefania Solmi,Carles Bó,Giulia Licini
标识
DOI:10.1002/adsc.201800050
摘要
Abstract The aerobic oxidative C−C bond cleavage of vicinal diols catalyzed by vanadium amino triphenolates is described. Our results show that C−C bond cleavage can be performed in different solvents, under an air or oxygen atmosphere, with a large variety of glycols (cyclic or linear, with aromatic or aliphatic substituents) affording the corresponding carbonyl derivatives with high chemoselectivity. Reactions can be performed with as little as 10 ppm of catalyst reaching TON up to 81,000 and TOFs of up to 4150 h −1 . A reaction mechanism, rationalized by density functional theory calculations, is also proposed. magnified image
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