Abstract
An efficient and green methodology for the synthesis of tetrahydroquinoline spiro[5.6] compounds by visible-light-induced sp3C–H functionalization reactions of alkyl amines has been developed. The advantages of this protocol include inexpensive photocatalysts, high diastereoselectivity, transition-metal-free properties, and wide-scope substrates.
| Original language | English |
|---|---|
| Pages (from-to) | 9843-9848 |
| Number of pages | 6 |
| Journal | Organic Letters |
| Volume | 27 |
| Issue number | 36 |
| DOIs | |
| State | Published - 12 Sep 2025 |