Abstract
The light-promoted potential of ortho -azidocinnamoyl compounds is evaluated for heterocycle synthesis. Depending on the nature of the solvent, 2-acylated indoles were obtained under aprotic conditions, whereas the use of a protic medium led to 2-substituted quinolines. The synthetic significance of this metal-free method is that, by simply changing the solvent, the reaction outcome can be directed towards different key heterocyclic scaffolds.
Original language | English (US) |
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Pages (from-to) | 2614-2618 |
Number of pages | 5 |
Journal | Synlett |
Volume | 28 |
Issue number | 19 |
DOIs | |
State | Published - Dec 1 2017 |
Keywords
- azides
- indoles
- nitrenes
- photochemistry
- quinolines
- rearrangement
- solvent effect
ASJC Scopus subject areas
- Organic Chemistry