supported by the National Natural Science Foundation of China(22022704,21977097,22271291),Chinese Academy of Sciences。
The central-to-axial chirality conversion represents a fascinating class of chemical processes consisting of the destruction of stereogenic centers and the simultaneous installation of axial chiral elements,which prov...
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...
the Natural Science Foundation of Zhejiang Province(LY22B020001);the Zhejiang Public Welfare Public Research Program(LGC22B010001);the National Natural Science Foundation of China(32201238)is greatly acknowledged.
Functionalized free radical addition/cyclization reactions represent an efficient way for introducing new functionality or coupling fragments to molecules.Ynones are good regional selectivity radical acceptors in orga...
funded by the Scientific Research Fund of Hunan Provincial Education Department(No.22B0435).
A facile and efficient electrochemical method for sustainable constructing both selanyl phenanthrenes and selanyl polycyclic heteroaromatics(32 examples,71%-97%yields)through the radical annulation of 2-alkynyl biaryl...
supported by Guangdong Basic and Applied Basic Research Foundation (2019A1515011743);the Pearl River talent program of Guangdong Province (Youth Top-Notch Talent,2017GC010302);Jinan University
A mild and practical protocol for selectively time-dependent dehydrogenative C–C coupling,as well as tandem couplingcyclization reaction between indoles or/and other heteroaromatics via electrochemically oxidative pr...
supported by the National Natural Science Foundation of China(21925108,22171225)。
Transition metal-catalyzed diamination by hydroxylamines is a common approach for making three-membered aziridines,while its use for building the larger N-heterocycles is still underdeveloped.Herein,we report an effic...
Financial support from National Natural Science Foundation of China(nos.21772046 and 2193103)is gratefully acknowledged.
An unprecedented atroposelective Catellani reaction between phosphine oxide-containing aryl bromides,aryliodides,and nucleophiles for the construction of phosphine-containing biaryl atropisomers was established using ...
The authors gratefully acknowledge financial support from the NSFC(nos.21772170 and 21925109 for B.-F.S.and no.21901228 for G.L.);Outstanding Young Talents of Zhejiang Province High-level Personnel of Special Support(no.ZJWR0108 for B.-F.S.).
The merging of C-H and C-C bond cleavage into one single chemical process remains a daunting challenge,especially in an asymmetric manner.Herein,a Pd(Ⅱ)-catalyzed enantioselective tandem C-H/C-C activation for the sy...
The well-defined conformational properties of axially chiral compounds bring extraordinary values to an assortment of bioactive molecules,advanced materials,organocatalysts as well as chiral ligands in asymmetric tran...
This project was generously supported by the National Natural Science Foundation of China(No.21662025);Beijing National Laboratory for Molecular Sciences(No.BNLMS201811).
of main obse rvation and conclusion An efficient strategy for the formation of alkenyl-functionalized spirocarbocyclic scaffolds from alkyne-containing phenol-based biaryls via sequential iodine-induced cyclization/de...