Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

1.5- Cyclooctadiene homogeneous catalysis

Such diene complexes can be used to prepare homogeneous hydrogenation catalysts in situ, especially where a variable tertiary phosphine/rhodium ratio is required3 or where an asymmetric tertiary phosphine is employed for asymmetric synthesis.4 The cyclooctadiene complex is also the starting point for the preparation a number of complexes of the type [Rh(l, 5-C8H12)L2]+ (L represents a variety of P— and N— donor ligands) of interest in homogeneous catalysis.s... [Pg.218]

Hassan A. Tayim and J. C. Bailar, Jr., Homogeneous Catalysis in the Reactions of Olefinic Substances. VIII. Isomerization of 1,5-Cyclooctadiene with Dichlorobis-(triphenyl-phosphine)platinum(II), J. Am. Chem. Soc. 89 3420 (1967). [Pg.349]

A 4 molar excess of fris-o-tolylphosphite in the presence of the supported nickel—carbonyl catalyst gave a 92% yield in cyclooctadiene, a result identical to that obtained in homogeneous catalysis. Again, the rate is three times lower than... [Pg.180]


See other pages where 1.5- Cyclooctadiene homogeneous catalysis is mentioned: [Pg.98]    [Pg.17]    [Pg.9]    [Pg.373]    [Pg.2150]    [Pg.237]   
See also in sourсe #XX -- [ Pg.8 , Pg.450 ]




SEARCH



1.3- Cyclooctadien

Cyclooctadienes

Cyclooctadienes 1.3- Cyclooctadiene

Cyclooctadienes homogeneous catalysis

Cyclooctadienes homogeneous catalysis

Homogeneous catalysis

Homogenous catalysis

© 2024 chempedia.info