化学
钌
催化作用
烯丙基重排
选择性
胺气处理
酒
溶剂
Noyori不对称加氢
有机化学
药物化学
作者
Bernhard M. Stadler,Pim Puylaert,Justus Diekamp,Richard van Heck,Yuting Fan,Anke Spannenberg,Sandra Hinze,Johannes G. de Vries
标识
DOI:10.1002/adsc.201701607
摘要
Abstract Ru(NNS)(PPh 3 )Cl 2 (NNS=2‐(methylthio)‐N‐(pyridin‐2‐yl‐methyl)ethan‐1‐amine) was employed in the hydrogenation of α,β‐unsaturated esters, reaching selectivities for the allylic alcohol up to 95% in the hydrogenation of iso‐butylcinnamate. In addition, several ester substrates were hydrogenated with catalyst loadings as low as 0.05 mol%. Surprisingly, selectivity of the hydrogenation of the C=O vs the C=C bonds strongly depends on the solvent. magnified image
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