Abstract
P-stereogenic phosphorus compounds are a ubiquitous and critically important class of chiral ligands in asymmetric catalysis. Methods for catalytic asymmetric synthesis via a step- and atom-economic way are still very limited. We herein disclose a protocol of phosphinate-directed iridium-catalyzed enantioselective ortho-H borylation to construct P-stereogenic phosphorus compounds. A number of functional groups could be well tolerated to afford optically active diarylphosphinates with good to excellent enantioselectivities (up to 92% ee). We also demonstrate the synthetic utilities of the obtained borylated products, including the synthesis of precursors for chiral phosphine ligands.
| Original language | English |
|---|---|
| Pages (from-to) | 13445-13451 |
| Number of pages | 7 |
| Journal | ACS Catalysis |
| Volume | 11 |
| Issue number | 21 |
| DOIs | |
| State | Published - 5 Nov 2021 |
| Externally published | Yes |
Keywords
- Asymmetric catalysis
- C-H activation
- Organoboron
- P-chiral phosphorus
- Synthetic methods