Financial support from National Natural Science Foundation of China(Nos.21931013 and 22271105);Natural Science Foundation of Fujian Province(No.2022J02009);Open Research Fund of School of Chemistry and Chemical Engineering,Henan Normal University;the Instrumental Analysis Center of Huaqiao University for analysis support;the Subsidized Project for Cultivating Postgraduates’Innovative Ability in Scientific Research of Huaqiao University。
A practical method for the construction of difluoromethylene-containing 1,4-thiazine moieties using readily available diethyl bromodifluoromethanephosphonate(BrCF_(2)PO(OEt)_(2))as difluorocarbene precusor has been de...
supported by the National Key Research and Development Program of China(2022YFA1506100);Shenzhen Science and Technology Program(JCYJ20220818100604009);Guangdong Basic and Applied Basic Research Foundation(2021A1515010105,2023A1515010601)。
Methylenecyclopropanes are among the most robust building blocks in synthetic chemistry,but the study on(difluoromethylene)-cyclopropanes is rather limited,because of the difficulty in the synthesis of these compounds...
the National Natural Science Foundation of China(NSFC,Nos.21877020,22007020);Natural Science Foundation of Guangdong Province(No.2019A1515010935);Science and Technology Program of Guangzhou(No.202102020615)for financial support on this study。
By developing gem-difluoromethylene allenes as viable partners,regiocontrolled Rh(Ⅲ)-catalyzed redoxneutral C-C coupling/C-N cyclization has been realized to build the pyridin-2(1H)-one motifs with the embedment of a...
supported by the National Natural Science Foundation of China (Nos.21772142,21901181 and 21961142015);the National Key Research and Development Program of China (No.2019YFA0905100);Tianjin Municipal Science & Technology Commission (No.19JCQNJC04700);the CNRS in France。
Three bench-stable difluoromethylene phosphonate hydrazones were prepared from simple diethyl(difluoromethyl)phosphonate within two steps in good yields. The [3 + 2] cycloaddition reaction of these diazo precursors wi...
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...
A Cul-catalyzed three-component coupling of trifluoromethyl ketone N-tosylhydrazones, alkynes and azides has been developed. The reaction represents a straightforward method to access difluoromethylene substituted 1,2...
financial supports from the National Natural Science Foundation of China(Nos.21472126,21172148,21302128)
A convenient and efficient approach for difluoroalkyl-containing γ-hutyrolactones via the radical addition reaction of iododifluoromethyl ketones with 4-pentenoic acids initiated by AIBN in CH3CN at 60 ℃ was reporte...
the National Natural Science Foundation of China (Nos. 21272036, 21332010);the National Basic Research Program of China (No. 2012CB21600)
A novel gem-difluoromethylenated castanospermine analogue B was designed and synthesized, starting from 3-bromo-3,3-difluoropropene and L-(-)-malic acid. The key steps involve substitution cyclization reaction and R...
The authors thank the National Natural Science Foundation of China(NSFC)(Nos.21032006,21172240);the 973 Program of China(No.2012CBA01200);the Chinese Academy of Sciences for financial support.
Difluoromethylene phosphobetaine(Ph_(3)P^(+)CF_(2)CO_(2)^(-),PDFA),a known difluorocarbene reagent,was found to be able to efficiently trifluoromethylate terminal alkynes in the presence of Cu(I)and potassium fluoride...
We thank the National Natural Science Foundation of China for financial support(No.20572124).
β-Allenic α-difluoromethylenephosphonic acid monoesters were prepared under mild conditions for the first time by hydrolyzing the corresponding diethyl phosphonates in aqueous sodium hydroxide solution.