Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 19, Issue 42, Pages 9177-9181Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ob01799c
Keywords
-
Categories
Funding
- National Natural Science Foundation of China [22071211]
- Science and Technology Planning Project of Hunan Province [2019RS2039]
- Hunan Provincial Natural Science Foundation of China [2020JJ3032]
Ask authors/readers for more resources
In this study, a visible-light-induced photoredox Minisci alkylation reaction of N-heteroarenes with ethyl acetate was successfully achieved. The low-toxic ethyl acetate was employed as the alkylation reagent for the first time, leading to smooth reactions of 4-quinazolinones, quinolines, and pyridines. Mechanistic studies revealed that LiBr significantly enhanced the efficiency of the reaction through mediating hydrogen atom transfer.
A visible-light-induced photoredox Minisci alkylation reaction of N-heteroarenes with ethyl acetate has been reported. The low-toxic ethyl acetate was used for the first time as an alkylation reagent. Hence, 4-quinazolinones, quinolines and pyridines reacted smoothly in the current reaction system. Mechanistic studies indicate that LiBr plays a key role to dramatically improve the efficiency of the reaction by the mediation of hydrogen atom transfer.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available