Journal
ORGANIC LETTERS
Volume 17, Issue 18, Pages 4554-4557Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b02270
Keywords
-
Categories
Funding
- Carl Trygger's Foundation [13:338, 14:359]
Ask authors/readers for more resources
An efficient, mild, and metal-free arylation of nitro-alkanes with diaryliodonium salts has been developed, giving easy access to tertiary nitro compounds. The reaction proceeds in high yields without the need for excess reagents and can be extended to alpha-arylation of nitroesters. Nitroalkanes were selectively C-arylated in the presence of other easily arylated functional groups, such as phenols and aliphatic alcohols.
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