化学选择性
三氟乙酸
催化作用
化学
氢化物
烯丙基重排
有机化学
醛
催化循环
原位
药物化学
组合化学
氢
作者
Gerrit Wienhöfer,Felix A. Westerhaus,Kathrin Junge,Ralf Ludwig,Matthias Beller
标识
DOI:10.1002/chem.201300660
摘要
Abstract A selective iron‐based catalyst system for the hydrogenation of α,β‐unsaturated aldehydes to allylic alcohols is presented. Applying the defined iron–tetraphos complex [FeF(L)][BF 4 ] (L=P(PhPPh 2 ) 3 ) in the presence of trifluoroacetic acid a broad range of aldehydes are reduced in high yields using low catalyst loadings (0.05–1 mol %). Excellent chemoselectivity for the reduction of aldehydes in the presence of other reducible moieties, for example, ketones, olefins, esters, etc. is achieved. Based on the in situ detected hydride species [FeH(H 2 )(L)] + a catalytic cycle is proposed that is supported by computational calculations.
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