Asymmetric Hydrosilylation of 1-Alkenes Catalyzed by Palladium–MOP
- 1 March 1995
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 68 (3), 713-722
- https://doi.org/10.1246/bcsj.68.713
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- Palladium-catalyzed asymmetric arylation of 2,3-dihydrofuran with phenyl triflate. A novel asymmetric catalysis involving a kinetic resolution processOrganometallics, 1993
- Asymmetric catalysis. Production of chiral diols by enantioselective catalytic intramolecular hydrosilation of olefinsJournal of the American Chemical Society, 1992
- Crystal and molecular structure of an asymmetric hydrogenation catalyst-substrate adduct, .DELTA.-bis(tiglato){(R)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl}ruthenium(II), [RuII(BINAP)(O2CCMe:CHMe)2]Organometallics, 1991
- Catalytic asymmetric hydroboration of styrenesJournal of the American Chemical Society, 1989
- Silafunctional compounds in organic synthesis. 35. Silafunctional .alpha.,.beta.-epoxy silanes. Transformation into erythro- and threo-1,2-diol skeletons and its application to the synthesis of (.+-.)-exo-brevicominThe Journal of Organic Chemistry, 1987
- Bis[(R)‐(+)‐binap]rhodium(I) Perchlorate, a Highly Efficient Catalyst for the Asymmetric Isomerization of AllylaminesAngewandte Chemie-International Edition, 1985
- Rapid separation of organic mixtures by formation of metal complexesThe Journal of Organic Chemistry, 1975
- Asymmetric homogeneous hydrosilylation with platinum(II) complexes of chiral phosphinesJournal of the American Chemical Society, 1971
- CVII.—Investigations on the dependence of rotatory power on chemical constitution. Part VI. The optical rotatory power of methyl-tert.-butyl-, methylbenzyl-, methylphenylethyl- and methyl-α-naphthyl-carbinolsJournal of the Chemical Society, Transactions, 1914
- CCVII.—Investigations on the dependence of rotatory power on chemical constitution. Part IV. The rotations of the normal secondary alcohols of the formula C2H5·CH(OH)·RJournal of the Chemical Society, Transactions, 1913