Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 75, Issue 21, Pages 7502-7504Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo1017525
Keywords
-
Categories
Funding
- Guangzhou Institutes of Biomedicine and Health (GIBH)
- Guangzhou Municipal Foundation for Science and Technology [2010Y1-C241]
Ask authors/readers for more resources
Diversified 2-alkoxy- and 2-aroxy-3-substituted quinolines were synthesized from o-alkynylaryl isocyanides and alcohols and phenols promoted by DABCO, respectively. The reaction was initiated by nucleophilic addition of DABCO to isocyanide and subsequent cycliztion, leading to a DABCO-quinoline-based adduct as the reactive intermediate, followed by substitution of the DABCO moiety with oxygenated nucleophiles.
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