| Literature DB >> 26768823 |
Zhikun Zhang1, Weizhi Yu1, Chenggui Wu1, Chengpeng Wang1, Yan Zhang1, Jianbo Wang2,3.
Abstract
A transition-metal-free difluoromethylenation of diazo compounds that proceeds under mild conditions has been developed and is based on the use of TMSCF2 Br as the difluoromethylene source and tetrabutylammonium bromide (TBAB) as the promoter. The chemoselective formal carbene dimerization reaction is achieved owing to the electronic properties and the relative stability of the difluorocarbene intermediate.Entities:
Keywords: carbenes; diazo compounds; difluorocarbene; fluorine; hydrazones
Year: 2015 PMID: 26768823 DOI: 10.1002/anie.201509711
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336