STEREOCHEMISTRY OF HYDROGENATION ON HOMOGENEOUS PHASE OF BICYCLIC METHYLENIC OLEFINS CATALYZED BY TRIS(TRIPHENYLPHOSPHINE)HALOGENRHODIUM

被引:14
作者
ROUSSEAU, C
EVRARD, M
PETIT, F
机构
[1] Laboratoire de Chimie Organique Appliquée, ERA CNRS no 070458, ENSCL, 59650 Villeneuve D'Ascq
来源
JOURNAL OF MOLECULAR CATALYSIS | 1979年 / 5卷 / 03期
关键词
D O I
10.1016/0304-5102(79)80054-1
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The stereochemistry of the reduction of 2-methylene bicyclo [2.2.1]- heptanes, more or less methylated, catalyzed by Rh(Pφ3)3X depends mainly on the substitution reaction {A figure is presented} leading to the formation of two (π-olefin)-metal complexes, precursors of endo-and exo- 2-methyl bicyclo[2.2.1] heptanes. Identical results were obtained when the same hydrogenations were carried out using a solid catalyst such as PtO2. © 1979.
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页码:163 / 173
页数:11
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