support by the National Natural Science Foundation of China(22101157)is gratefully acknowledged;We are very grateful to Prof.Xiao Shen(Wuhan University,China)for helpful discussion.
The pursuit of sustainable and environmentally benign synthetic methods continues to challenge organic chemists. Herein, we introduce a magnetoredox system for tri- and difluoromethylation of isocyanides and N-arylacr...
the financial support from the National Natural Science Foundation of China(No.21503161);the Key Research&Development Project in Shaanxi Province(No.2017ZDXM-GY-040);the Doctoral Scientific Research Foundation of Xi'an Polytechnic University(No.107020336).
We reported for the first time that ethyl bromodifluoroacetate directly reacts with azaindole without transition metal catalysis to produce a difluoromethyl protected 5-aldehyde group product in one step.It is worth m...
The authors thank the National Natural Science Foundation of China(Nos.21421002,21672242,21971252);the Key Research Program of Frontier Sciences(CAS)(QYZDJSSW-SLH049);Youth Innovation Promotion Association CAS(2019256);Shanghai Research Institute of Chemical Industry Co.,Ltd.(SKL-LCTP-201802)for financial support.
Summary of main observation and conclusion CF3S,CF3 and HCF2 groups have been identified as valuable functionalities for drug development.Despite significant accomplishments in the trifluoromethylthiolation,trifluorom...
We gratefully acknowledge the financial support from the National Natural Science Foundation of China(Nos.21772202,21701073,21831008);Beijing Municipal Science&Technology Commission(No.Z181100004218004);Beijing National Laboratory for Molecular Sciences(No.BNLMS-CXXM-201901);the Fundamental Research Funds for the Central Universities(lzujbky-2017-12 and lzujbky-2019-kb06).
Summary of main observation and conclusion Herein,unprecedented rhenium-catalyzed decarboxylative oxytri-/difluoromethylation and Heck-type trifluoromethylation of styrenes have been developed by using hypervalent iod...
The authors gratefully acknowledge the financial support from National Natural Science Foundation of China (Nos. 21625206, 21632009, 21572258, 21572259, 21421002, 21772098) and the Strategic Priority Research Program of the Chinese Academy of Sciences (No. XDB20000000) for financial support.
This work was financially supported by the National Natural Science Foundation of China (Nos. 21425208, 21672238, 21332010, and 21421002), the Strategic Priority Research Program of Chinese Academy of Sciences (No. XDB20000000), and SIOC.
Although bromodifluoromethane (BrCF2H) is a simple and readily available fluorine source, direct formation of difluoromethylated arenes with BrCF2H has not been reported. Herein, we describe an efficient method to a...
The Nationa authors gratefully acknowledge the financial support from Natural Science Foundation of China (21625206, 21632009, 21372247, 21572258, 21572259, 21421002) and the Strategic Priority Research Program of the Chinese Academy of Sciences (XDB20000000) and the Syngenta Ph.D. Fellowship (Y. Gu and C. Lu).
Highly regiodivergent copper-catalyzed allylic/propargylic difluoromethylation reactions by employing different ligands are described. When 5,6-dimethyl-1,10-phenanthroline was used as the ligand, exclusively α-diflu...
A novel iodonium-ylide compound 2 that appends a trifluoromethylthio (SCF3) group is disclosed as a new, shelf-stable electrophilic trifluoromethylation reagent. Unlike known shelf-stable electrophilic trifluorometh...
Projrct supportted by the National Natural Science Foundation of China (Nos. 20772144, 20825209, 20832008) and the Chinese Academy of Sciences (Hundreds-Talent Program and Knowledge Innovation Program).
Difluoromethyltri(n-butyl)ammonium chloride 1 was found to be an effective difluorocarbene reagent for O-, S-, N-, C-difluoromethylation under basic conditions. It is particularly remarkable that, when only 1.2 equi...