financial support provided by the National Natural Science Foundation of China(Nos.21991123,21971036,21901036);the Shanghai Rising-Star Program(No.20QA1400200)。
We report a Ni-catalyzed three-component cross-electrophile coupling of alkynes with alkenyl halides and fluoroalkyl halides to generate fluoroalkyl-incorporated 1,3-dienes.This mild and operationally simple protocol ...
the National Natural Science Foundation of China (No. 21901191);the Fundamental Research Funds for the Central Universities and Wuhan University for financial support
Herein, we report an unprecedented regiospecific oxidative Mizoroki-Heck type reaction for the synthesis of α-difluoromethyl homoallylic alcohols. The reaction shows broad substrate scopes and high functional group t...
supported by the Natural Science Foundation of China(Nos.22122104,21933004 and 21702098).
Although fluorobis(phenylsulfonyl)methane(FBSM)and its cyclic analog 2-fluoro-1,3-benzodithiole-1,1,3,3-tetraoxide(FBDT)possess similar physicochemical properties,Shibata et al.found that FBSM failed to undergo nucleo...
Abstracts: In the presence of detonate, excess per(poly)fluoroalkyl iodide reacted with parasubstituted phenolates to provide his-por(poly)fluoroalkyl substituted phenols in fair to good yields.