Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 79, Issue 3, Pages 1084-1092Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo402540j
Keywords
-
Categories
Funding
- Natural Science Foundation of China [21176223]
- National Natural Science Foundation of Zhejiang [LY13B020016]
- Key Innovation Team of Science and Technology in Zhejiang Province [2010R50018]
Ask authors/readers for more resources
We report a novel molecular iodine-catalyzed 1,3-dipolar cycloaddition/oxidation/aromatization cascade process with hydrogen peroxide as the terminal oxidant for the construction of pyrrolo[2,1-a]isoquinolines. The product pyrrolo[2,1-a]isoquinolines were obtained from reactions between simple, readily available dipolarophiles and tetrahydroisoquinolines in moderate to excellent yields without the need for a metal 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