financial support from the National Natural Science Foundation of China(Nos.22071062,22001077 and 22271096);Guangdong Science and Technology Department(Nos.2021A1515012331,2023A1515011001);the Fundamental Research Funds for the Central Universities(No.2022ZYGXZR016);South China University of Technology for start-up funds。
Axially chiral binaphthol have achieved great success in asymmetric catalysis.Compared toα-binaphthol,axially chiral aryl-β-naphthol are far less reported.Here,we report a method of asymmetric catalysis to construct...
Z.-M.Chen thanks National Natural Science Foundation of China(22071149,21871178);Natural Science Foundation of Shanghai(23ZR1428200);financial support.H.Ke thanks Natural Science Foundation of Jiangxi Province(20202ACBL213005)for financial support.
Chiral BINAM-derived selenide/achiral acid co-catalyzed atroposelective electrophilic sulfenylation of pyrrole derivatives has been realized for the first time.A variety of C-N axially chiral sulfur-containing pyrrole...
the Natural Science Foundation of Jiangsu Province(BK20221309);the National Natural Science Foundation of China(21602105).
Axially chiral biaryls represent the most important class of atropisomers,and they widely exist in natural products and biologically active molecules.They also constitute a unique scaffold for chiral ligands and catal...
We thank the financial support from the Program for Young Talents of Shaanxi Province(5113200043);the Fundamental Research Funds for the Central Universities.
We report herein an unprecedented N-heterocyclic carbene-catalyzed formal[3+3]annulation of ynals with N-Ts indolin-3-ones under the oxidation condition affording the functionalized pyrano[3,2-b]indol-2-ones.The alkyn...
Herein,we report an asymmetric two-component alkenyl Catellani reaction for the construction of C—N axial chirality through a palladium/chiral norbornene cooperative catalysis and an axial-to-axial chirality transfer...
supported by Taishan Scholar Youth Expert Program in Shandong Province (tsqn201909096);National Natural Science Foundation of China (22371152);Shandong Provincial Natural Science Foundation Project (ZR2023JQ006,ZR2022MB021);the startup fund from Qingdao University.
Atroposelective synthesis of N-N atropisomers is an emerging area but remains underexplored;in particular,the synthesis of N-N benzimidazole atropisomers is still unprecedented.Herein,the first enantioselective synthe...
financial supports from National Natural Science Foundation of China(92056102);the Natural Science Foundation of Fujian Province(2023J011395).
The widespread applications of atropisomeric compounds have led to an increasing demand for their synthesis.Rather than synthesizing different functionalized atropisomers individually,an attractive alternative is to i...
the funding support of NSFC(Nos.22031004,21921003,21901043);Shanghai Municipal Education Commission(No.20212308).
Atropisomeric anilides are one of important C-N axially chiral compounds.Compared with the A/-terminal functionalization to prepare such compounds,C-terminal functionalization strategies have been rarely reported.We d...
We are grateful for the financial support from NSFC(Grant No.21831007).
A highly efficient kinetic resolution of racemic thioanilide atropisomers via C(sp^(3))-H arylation has been achieved by a hybrid palladium catalyst bearing an anionic chiral Co^(Ⅲ)-complex and a phosphoramidite liga...
We are grateful for financial support from the National Natural Science Foundation of China(Nos.21772069 and 21831007);the Postgraduate Research&Practice Innovation Program of Jiangsu Province(No.KYCX20_2235);the Natural Science Foundation of JSNU(No.19XSRX013)。
Atroposelective construction of axially chiral alkene-heteroaryl scaffolds is highly desired but challenging.In this work,we established an atroposelective construction of axially chiral alkene-indole scaffolds via th...