supported by the National Key Research and Development Program of China(2022YFA1502902);the National Natural Science Foundation of China(22371215,22222111,21971198);the Guangdong Basic and Applied Basic Research Foundation(2022A1515012614);the Large-scale Instrument and Equipment Sharing Foundation of Wuhan University;China Postdoctoral Science Foundation(2022M722451)for the financial support。
Construction of axially chiral 1-azafluorenes via nickel-catalyzed[2+2+2]cycloaddition of alkynes and(o-alkynyl)benzyl nitriles is described.This strategy enables enantioselective discrimination of two sterically simi...
supported by the National Natural Science Foundation of China(No.22171021);Yanjing Young Scholar Candidate Program of Capital Normal University,Capacity Building for SciTech Innovation-Fundamental Scientific Research Funds.
By using a perylene diimine(PDI)syn-atropisomer as highly preorganized precursor,we successfully constructed a visible-light-active organic macrocycle PDI-M.The formation of macrocyclic structure effectively avoids se...
Many therapeutic drugs are racemates;i.e. they are chiral molecules consisting of “left”- and “right-handed” enantiomers (stereoisomers that are mirror images of each other, and are non-superimposable). In some ca...
A visible light accelerated C-H functionalization reaction in palladium-catalyzed arylation of vinyl arenes with diaryliodonium salts is reported in the absence of additional photosensitizer. The kinetic isotope effe...
In the pharmaceutical industry, the analysis of atropisomers is of considerable interest from both scientific and regulatory perspectives. The compound of interest contains two stereogenic axes due to the hindered rot...
Supported by the National Natural Science Foundation of China(No.20806025)
Four "picket fence" porphyrin atropisomers were respectively synthesized from the four corresponding atropisomers of meso-tetra(o-aminophenyl)porphyrin that had been chromatographed on a column eluted with petrole...