烯丙基重排
化学
催化作用
有机化学
醛
双键
联苯
戒指(化学)
催化加氢
反应条件
酒
脂肪族化合物
作者
Jie Wang,F. Yang,Linping Li,Jia-Qi Han,Jian‐Hua Xie,Qi‐Lin Zhou
标识
DOI:10.1021/acs.joc.5c02388
摘要
Ir-BiphPAP catalysts, featuring biphenyl-derived pyridine-aminophosphine ligands, are reported for the selective hydrogenation of α,β-unsaturated aldehydes. These Ir-PNN catalysts enable the highly active and selective hydrogenation of the C═O bond of α,β-unsaturated aldehydes to afford allylic alcohols. In particular, catalyst 1b, incorporating 5,5'-di-tert-butyl groups on the biphenyl ring of the ligand, effectively converts a variety of α,β-unsaturated aldehydes into allylic alcohols with high yields and excellent selectivity, and the turnover number is as high as 78,000.
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