Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 21, Issue 42, Pages 8471-8476Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d3ob01100c
Keywords
-
Categories
Ask authors/readers for more resources
A visible light induced C-3 thiocyanation of imidazo[1,2-a]pyridines and various other heterocycles was achieved using a naphthalimide based photoredox catalyst. Electron withdrawing and donating groups at different positions of the imidazo[1,2-a]pyridine ring were well tolerated, expanding the substrate accessibility. This method shows great potential for the synthesis of diverse sulfur-containing compounds.
A visible light induced C-3 thiocyanation of imidazo[1,2-a]pyridines by using a naphthalimide based photoredox catalyst has been reported. Tolerance of electron withdrawing and donating groups at different positions of the imidazo[1,2-a]pyridine ring led to a wide substrate accessibility of this method. This methodology is further reproducible with other heterocycles like benzo[d]imidazo[2,1-b]thiazoles, indoles, azaindoles, and anilines. A visible light induced C-3 thiocyanation of imidazo[1,2-a]pyridines and various other heterocycles (benzo[d]imidazo[2,1-b]thiazoles, indoles, azaindoles, and anilines) was performed using a naphthalimide based photoredox catalyst.
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