化学
催化作用
不对称氢化
基质(水族馆)
药物化学
铑
晶体结构
立体化学
有机化学
对映选择合成
海洋学
地质学
作者
Hans‐Joachim Drexler,Wolfgang Baumann,Anke Spannenberg,Christine Fischer,Detlef Heller
标识
DOI:10.1016/s0022-328x(00)00756-7
摘要
Induction periods in the asymmetric hydrogenation of prochiral olefins with five-membered chelates of the type [Rh(PP)(diolefin)]BF4 originate from the parallel-running hydrogenation of the prochiral substrate and the diolefin that enters the system as a constituent of the precatalyst. Reactivities towards the most commonly used diolefins COD or NBD can differ by three powers of ten. X-ray crystal structure analyses of [Rh((S,S)-Et-DuPHOS)(NBD)]BF4 and of [Rh((R,R)-Et-DuPHOS)(COD)]BF4 imply that a recently discussed relation between the sense of rotation of the diolefin in the precatalyst (clockwise or anticlockwise twist) is not very likely.
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