Efficient Enantioselective Hydrosilylation of Ketones Catalyzed by Air Stable Copper Fluoride−Phosphine Complexes
- 20 November 2001
- journal article
- letter
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 3 (25) , 4111-4113
- https://doi.org/10.1021/ol0169170
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Hydrosilylation of aldehydes and ketones catalyzed by [Ph3P(CuH)]6Journal of Organometallic Chemistry, 2001
- Synthesis of β-Alkyl Cyclopentanones in High Enantiomeric Excess via Copper-Catalyzed Asymmetric Conjugate ReductionJournal of the American Chemical Society, 2000
- An efficient protocol for the reduction of ketones with tin(II) complexes and PMHSTetrahedron Letters, 2000
- Enantioselective Reduction of Ketones by Polymethylhydrosiloxane in the Presence of Chiral Zinc CatalystsJournal of the American Chemical Society, 1999
- Conjugate reduction of α,β-unsaturated ketones with hydrosilane mediated by copper(I) saltTetrahedron, 1999
- The influence of the catalyst preparation protocol and silane structure on the rate and enantioselectivity of ansa-titanocene catalysed hydrosilation of prochiral ketonesInorganica Chimica Acta, 1998
- Titanocene-Catalyzed Reduction of Lactones to LactolsThe Journal of Organic Chemistry, 1997
- An Inexpensive Air-Stable Titanium-Based System for the Conversion of Esters to Primary AlcoholsThe Journal of Organic Chemistry, 1995
- Simplified, “one-pot” procedure for the synthesis of [(Ph3P)CUH]6, a stable copper hydride for conjugate reductionsTetrahedron Letters, 1988