Abstract
A synthetic approach to quinindoline derivatives by the Cu-catalyzed dual cyclization has been developed. This catalytic reaction is a practical method for the systematic synthesis of quinindoline core structure, which contains a limited-step synthetic strategy and can tolerant a wide variety of substituents. In addition, the mechanistic study reveals that the reaction initiates from a Lewis acid accelerated addition of aniline to nitrile and provides the indole substructure, and then the subsequent Cu-catalyzed C-N coupling reaction furnishes the quinoline subunit and affords the quinindoline structure.
| Original language | English |
|---|---|
| Article number | 5303 |
| Journal | Molecules |
| Volume | 25 |
| Issue number | 22 |
| DOIs | |
| Publication status | Published - 2020 Nov 1 |
Keywords
- N-heterocycle
- copper-catalyzed
- cyclization
- natural alkaloid
- quinindoline
ASJC Scopus subject areas
- Analytical Chemistry
- Chemistry (miscellaneous)
- Molecular Medicine
- Pharmaceutical Science
- Drug Discovery
- Physical and Theoretical Chemistry
- Organic Chemistry
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