Abstract
A dinuclear Co(ii) complex supported by a modular, tunable redox-active ligand system is capable of selective C-H amination to form indolines from aryl azides in good yields at low (1 mol%) catalyst loading. The reaction is tolerant of medicinally relevant heterocycles, such as pyridine and indole, and can be used to form 5-, 6-, and 7-membered rings. The synthetic versatility obtained using low loadings of an earth abundant transition metal complex represents a significant advance in catalytic C-H amination technology.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 6672-6675 |
| Number of pages | 4 |
| Journal | Chemical Science |
| Volume | 6 |
| Issue number | 11 |
| DOIs | |
| State | Published - 2015 |
All Science Journal Classification (ASJC) codes
- General Chemistry
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