Transition metal catalysis in fluorous media: extension of a new immobilization principle to biphasic and monophasic rhodium-catalyzed hydrosilylations of ketones and enones

被引:43
作者
Dinh, LV
Gladysz, JA
机构
[1] Univ Erlangen Nurnberg, Inst Organ Chem, D-91054 Erlangen, Germany
[2] Univ Utah, Dept Chem, Salt Lake City, UT 84112 USA
关键词
hydrosilylation; rhodium; catalyst recovery; fluorocarbon solvents;
D O I
10.1016/S0040-4039(99)01924-3
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The title protocol utilizes CF3C6F11 Solutions of ClRh[P(CH2CH2(CF2)(n-1)CF3)(3)](3) (n=6, 8; 0.8-0.2 mol%) and toluene (biphasic conditions, 60 degrees C) or hexanes or ether (monophasic conditions, 28-60 degrees C) solutions of PhMe2SiH and cyclic enones or ketones. Samples are cooled to room temperature or -30 degrees C, and simple organic/fluorous phase separations remove products from the catalyst, which can be directly reused without loss of activity. (C) 1999 Elsevier Science Ltd. All rights reserved.
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页码:8995 / 8998
页数:4
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