| Literature DB >> 24668854 |
Juanjuan Du1, Yaxi Yang, Huijin Feng, Yuanchao Li, Bing Zhou.
Abstract
A Rh(III) -catalyzed addition of aryl CH bonds to nitrosobenzenes, followed by cleavage of the resulting hydroxylamines in situ, has been reported. Different directing groups, such as N-based heterocycles and ketoximes, can be used in this CH amination process, providing valuable diarylamines in excellent yields. Most importantly, this process provides a new method for attaching arylamine groups to aromatic rings.Entities:
Keywords: CH activation; diarylamines; isatin; nitrosobenzenes; rhodium
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Year: 2014 PMID: 24668854 DOI: 10.1002/chem.201400221
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236