Abstract
We herein report an iridium-catalyzed enantioselective α-C(sp3)-H borylation of a wide range of azacycles. The combination of an iridium precursor and a chiral bidentate boryl ligand has been shown to effectively differentiate enantiotropic methylene C-H bonds from a single carbon center, affording a variety of synthetically useful azacycles from readily available starting materials with good to excellent enantioselectivities.
| Original language | English |
|---|---|
| Pages (from-to) | 12062-12068 |
| Number of pages | 7 |
| Journal | Journal of the American Chemical Society |
| Volume | 142 |
| Issue number | 28 |
| DOIs | |
| State | Published - 15 Jul 2020 |
| Externally published | Yes |