Journal
CHEMICAL COMMUNICATIONS
Volume 59, Issue 47, Pages 7216-7219Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d3cc00875d
Keywords
-
Categories
Ask authors/readers for more resources
A highly regio- and chemoselective three-component reaction between N-pyrimidyl indoles, dienes, and formaldehyde in the presence of a Co(iii) catalyst was demonstrated. The reaction scope was investigated using various indole derivatives to synthesize substituted homoallylic alcohols. Both butadiene and isoprene units were found to be compatible with this reaction. Various investigations suggested that the reaction mechanism involves C-H bond activation as a key step.
A highly regio- and chemoselective three-component assembling of N-pyrimidyl indoles with dienes and formaldehyde in the presence of a Co(iii) catalyst was demonstrated. The scope of the reaction was investigated with a variety of indole derivatives to synthesize substituted homoallylic alcohols. Both butadiene and isoprene units were compatible with the reaction. To understand the reaction mechanism, various investigations were carried out, and suggested the plausibility of a reaction mechanism involving C-H bond activation as a key step.
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