Abstract
Effective asymmetric reduction of alkyl phenyl, dialkyl and alkyl cyclohexyl ketones has been achieved via hydrosilylation, catalyzed by a rhodium(I) complex with optically active phosphine ligands using various hydrosilanes. A mechanism of the induction of asymmetry is proposed in view of the stereochemical course of the reaction.
| Original language | English |
|---|---|
| Pages (from-to) | 83-97 |
| Number of pages | 15 |
| Journal | Journal of Organometallic Chemistry |
| Volume | 122 |
| Issue number | 1 |
| DOIs | |
| State | Published - Dec 7 1976 |
Fingerprint
Dive into the research topics of 'Reduction of carbonyl compounds via hydrosilylation. II. Asymmetric reduction of ketones via hydrosilylation catalyzed by a rhodium(I) complex with chiral phosphine ligands'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver