Hydroformylation of 1-hexene under mild conditions catalyzed by various μ-pyrazolato dirhodium(I) complexes
- 1 August 1985
- journal article
- Published by Elsevier in Journal of Molecular Catalysis
- Vol. 31 (3) , 311-315
- https://doi.org/10.1016/0304-5102(85)85113-0
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Pyrazolyl-bridged iridium dimers. 5. Crystal and molecular structures of bis(cycloocta-1,5-diene)bis(.mu.-pyrazolyl)diiridium(I), its dirhodium(I) isomorph, and two bis(cycloocta-1,5-diene)diiridium(I) analogs incorporating 3,5-disubstituted .mu.-pyrazolyl ligandsOrganometallics, 1983
- Two-centre oxidative addition of hexafluorobut-2-yne to a bis(µ-pyrazolyl)di-iridium(I) complex leading to bridge-elimination via H-transfer from co-ordinated cyclo-octa-1,5-diene: X-ray crystal structure of a mixed-bridge, mixed-valence iridium dimer incorporating a 1–3,5,6-η-C8H11lignadJournal of the Chemical Society, Chemical Communications, 1983
- Transformation of 1,3-aminoalcohols to ketones on copperJournal of Molecular Catalysis, 1982
- Thiocarbonylrhodium complexes with pyrazolate-type ligandsJournal of Organometallic Chemistry, 1981
- Pyrazolate bridged dinuclear rhodium complexes. X-ray structure of [Rh(Pz)(CO)P(OPh)3]2Journal of Organometallic Chemistry, 1981
- Reactions of compounds of the type [(diene)RhX]2 (diene = cycloocta-1,5-diene, bicyclo[2.2.1]hepta-2,5-diene; X = Cl, Br) with tertiary phosphines and phosphitesInorganic Chemistry, 1970