1537171-88-2Relevant articles and documents
Highly selective gem -difluoroallylation of organoborons with bromodifluoromethylated alkenes catalyzed by palladium
Min, Qiao-Qiao,Yin, Zengsheng,Feng, Zhang,Guo, Wen-Hao,Zhang, Xingang
, p. 1230 - 1233 (2014)
A first example of Pd-catalyzed gem-difluoroallylation of organoborons using 3-bromo-3,3-difluoropropene (BDFP) in high efficiency with high α/γ-substitution regioselectivity has been developed. The reaction can also be extended to substituted BDFPs and has advantages of low catalyst loading (0.8 to 0.01 mol %), broad substrate scope, and excellent functional group compatibility, thus providing a facile route for practical application in drug discovery and development.