氢甲酰化
铑
化学
催化作用
选择性
芳基
有机化学
醛
烯烃纤维
组合化学
药物化学
烷基
作者
Holger Klein,Ralf Jackstell,Klaus‐Diether Wiese,Cornelia Borgmann,Matthias Beller
标识
DOI:10.1002/1521-3773(20010917)40:18<3408::aid-anie3408>3.0.co;2-a
摘要
Readily accessible and highly efficient: Substituted 2,2′-bis(diphenylphosphanylmethyl)-1,1′-binaphthyl (NAPHOS) ligands 1 can be readily prepared from 2,2′-bis(dichlorophosphanylmethyl)-1,1′-binaphthyl. Especially ligands with electron-withdrawing aryl substituents (for example, 3,4,5-F3C6H2 (instead of Ph), 1 a) show a remarkable high activity and n:i selectivity in the rhodium-catalyzed hydroformylation of internal olefins (see scheme).
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