Photochemical Synthesis of 1,4‐Dicarbonyl Containing Quinoxalin‐2(1H)‐Ones through Consecutive Photoredox Catalysis
Herein, we report a photochemical synthesis of 1,4‐dicarbonyl containing quinoxalin‐2(1H)‐ones through consecutive photoredox catalysed reactions. A wide range of C3‐modified quinoxalin‐2(1H)‐ones were obtained in 53–91% yields by this approach. Mechanistic studies including radical trapping, EPR st...
Saved in:
Published in: | Advanced synthesis & catalysis Vol. 366; no. 8; pp. 1833 - 1839 |
---|---|
Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Heidelberg
Wiley Subscription Services, Inc
23-04-2024
|
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Herein, we report a photochemical synthesis of 1,4‐dicarbonyl containing quinoxalin‐2(1H)‐ones through consecutive photoredox catalysed reactions. A wide range of C3‐modified quinoxalin‐2(1H)‐ones were obtained in 53–91% yields by this approach. Mechanistic studies including radical trapping, EPR studies, D‐labelling investigations, and many other control experiments well explained the proposed consecutive photoredox mechanism. |
---|---|
ISSN: | 1615-4150 1615-4169 |
DOI: | 10.1002/adsc.202301393 |