Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 79, Issue 5, Pages 2331-2336Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo500131h
Keywords
-
Categories
Funding
- TEQIP
- CSIR
Ask authors/readers for more resources
Oxidative arylation of naphthoquinones has been developed through combination of o-iodoxybenzoic acid with arylhydrazines under mild conditions at open atmosphere. Arylated naphthoquinones with different electronic properties were obtained in moderate to good yields. The postulated radical mediated mechanism is supported by radical trapping experiments. Developed protocol for direct arylation of naphthoquinones has been extended toward short, high yielding, and an effective synthesis of antitumor-antibiotic precursor such as benzocarbazoledione.
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