ChemInform Abstract: Copper(I) Salt Mediated 1,4-Reduction of α,β-Unsaturated Ketones Using Hydrosilanes.
✍ Scribed by A. MORI; A. FUJITA; Y. NISHIHARA; T. HIYAMA
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
✦ Synopsis
Copper(I) Salt Mediated 1,4-Reduction of α,β-Unsaturated Ketones Using Hydrosilanes. -The title reaction is carried out for several acyclic and cyclic α,β-unsaturated ketones in excellent yields. Sterically congested enones such as (Va) are recovered unchanged, a fact that can be applied in competition reactions.
-(MORI, A.
📜 SIMILAR VOLUMES
## Abstract Under optimized conditions, a variety of ketones undergo asymmetric 1,2‐reductions almost exclusively instead of the normally observed 1,4‐reductions in the presence of in situ‐generated CuH which is ligated with an optically active bisphosphane ligand.