区域选择性
氢甲酰化
铑
化学
部分
位阻效应
催化作用
选择性
组合化学
药物化学
立体化学
有机化学
作者
Shichao Yu,Xiaowei Zhang,Yongjun Yan,Chaoxian Cai,Liyan Dai,Xumu Zhang
标识
DOI:10.1002/chem.200903109
摘要
Abstract A new class of substituted tetraphosphane ligands has been developed and applied in the rhodium‐catalyzed regioselective hydroformylation of terminal olefins. The high regioselectivity (linear selectivity is above 97 % for 1‐octene and 1‐hexene) at high temperature (140 °C) shown by these tetraphosphane ligands is remarkable considering the low regioselectivity commonly observed under similar reaction conditions when other bisphosphane analogues are used. The steric and electronic effects of substituents on the diarylphosphane moiety have also been examined.
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