Abstract
Rhodium-catalysed enantioselective hydroboration of olefins is a valuable synthetic transformation, typically employing a chiral catalyst and an achiral borane source. The pertinent chemo-, regio- and enantioselectivity issues of this reaction are discussed. However, the main emphasis of this review is on the evolution of catalytic asymmetric hydroboration. This has primarily relied upon the development and application of chiral bidentate P,P and P,N ligands which have exhibited varying degrees of success in this transformation.
| Original language | English |
|---|---|
| Pages (from-to) | 609-631 |
| Number of pages | 23 |
| Journal | Advanced Synthesis and Catalysis |
| Volume | 347 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - Apr 2005 |
| Externally published | Yes |
Keywords
- Asymmetric catalysis
- Hydroboration
- Mechanistic studies
- P,N chiral ligands
- P,P chiral ligands
- Rhodium
Fingerprint
Dive into the research topics of 'The development of enantioselective rhodium-catalysed hydroboration of olefins'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver