supported by the National Key R&D Program of China(2021YFA1500100);the National Natural Science Foundation of China(21821002,22031012,and 22171282);the Science and Technology Commission of Shanghai Municipality(19590750400 and 21520780100)。
Imidazo[1,2-a]pyridines are present in numerous biologically active compounds as the core structural motif.Herein,we report an asymmetric interrupted Barton-Zard reaction of electron-deficient imidazo[1,2-a]pyridines ...
Financial support received from NSFC(Nos.21704048,22031005);the Department of Science and Technology of Shandong Province(No.ZR2020LFG014);the Taishan Scholars Constructive Engineering Foundation(No.tsqn20161031)is gratefully acknowledged.
Substa ntial progresses have bee n made toward the developme nt of meta I-free catalysts for stereoselective rin g-ope ning polymeriza-tion(ROP)of rac-lactide.Yet the discovery of organic catalysts effective at ambien...
the Spanish MINECO(projects RTI2018-095622-B-I00,RTI2018-095038-B-I00);the Catalan AGAUR(project 2017 SGR 238);the ERC under the EU FP7(ER C-Co 615954);European Unions Horizon 2020 research and innovation program under grant agreement No.685727,and European Structural Funds(S2018/NMT-4367).It was alsofunded by the CERCA Program/Generalitat de Catalunya.ICN2 is supported by the Severo Ochoa program from the Spanish MINECO(G rant No.SEV-2017-0706).
A well-established strategy to synthesize heterogeneous,metal-organic framework(MOF)catalysts that exhibit nanoconfinement effects,and specific pores with highly-localized catalytic sites,is to use organic linkers con...
the financial support from the National Natural Science Foundation of China(Nos.21572026 and 21702019);Advanced Catalysis and Green Manufacturing Collabo-rative Innovation Center,Changzhou University,and the Priority Academic Program Development of Jiangsu Higher Education Institutions.
A novel upper-rim functionalized calix[4]squaramide organocatalyst bearing bis-squaramide and cyclohexanediamine scaffolds was designed and prepared to catalyse a serial of asymmetric Michael addition of 1,3-dicarbo n...
The saccharide-based chiral bifunctional thiourea-phosphines were developed as chiral organocatalysts for the intramolecular Morita-Baylis-Hillman reaction of o^-formyl-enones. With only 2 tool% of thiourea-phosphine ...
the Fundamental Research Funds for the Central Universities (No.2042014kf0248) for support of this research
The asymmetric α-amination of 1,3-dicarbonyl compounds with dialkyl azodicarboxylates has been achieved by C2-symmetric BINOL-squaramide bearing multiple hydrogen bond donors to provide the desired products in excell...
support from the Na-tional Natural Science Foundation of China(Grant No.21272024).
Enantioselective synthesis of biologically active dihydropyrano[2,3-c]pyrazoles has been achieved through a squaramide-catalysed Michael addition/Thorpe-Ziegler type cyclization cascade reaction between arylidenepyra-...
financial support from the National Natural Science Foundation of China(Nos.21072010 and 21272024)
Enantioselective chlorination of b-keto esters and amides catalyzed by squaramide-linked bisoxazoline ligand–Cu(OAc)2complexes was investigated. The corresponding chlorinated products were obtained in excellent yie...
We are grateful for financial support from the National Natural Science Foundation of China(Grant No.21272024).
An efficient enantioselective cascade sulfa-Michael/Michael addition reaction of trans-3-(2-mercaptophenyl)-2-propenoic acid ethyl ester with nitroalkenes catalyzed by a chiral squaramide catalyst was disclosed.This c...