supported by the Natural Science Foundation of Zhejiang Province(LZ20B020001 and LY23B020004);the Ten Thousand Talents Plan of Zhejiang Province(2020R52021);the Leading Innovative and Entrepreneur Team Introduction Program of Zhejiang Province(2022R01007);the National Natural Science Foundation of China(22371262,22071218,and 22203076).
Comprehensive Summary A visible light photocatalytic[3+2]cycloaddition of alkynes with readily accessible organic iodides as the C3 synthon is developed herein.By merging halogen atom transfer(XAT)and hydrogen atom tr...
supported by the National Natural Science Foundation of China(22271007);the Peking University Shenzhen Graduate School;the State Key Laboratory of Chemical Oncogenomics;the Guangdong Provincial Key Laboratory of Chemical Genomics;the Shenzhen Bay Laboratory and Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs for JSZ。
Enantioselective domino alkenylation-alkynylation of olefins is achieved for the first time,using terminal alkynes directly as pronucleophiles.The new reaction enables facile construction of azacycles carrying quatern...
We are grateful for the financial support from the National Natural Science Foundation of China(22071028,21772024,21921003 to P.L.;21801044,22071122 to H.F.);We thank Dr.Huize Jing for her work on illustrations of rope acrobatics.
Cyclobutane derivatives have been recognized as useful structural motifs in organic synthesis and drug design.With the revival of photochemistry,the enantioselective synthesis of cyclobutane derivatives using[2+2]-cyc...
We are grateful for financial support from the National Natural ScienceFoundation of China(Nos.21871112 and 21971090).
Yne-allenes bearing both a C-C triple bond and an allene unit are a class of focal substrates in organic synthesis,in view of their structure diversity,.high reactivity and intermediate variety in the past years.Engag...
We are grateful for financial support from the National Natural Science Foundation of China(Nos.21871112 and 21971090);the Science and Technology of Xuzhou(KC21022)。
Molecular scaffolds endowed with all-carbon quaternary stereocenter are ubiquitous in natural products and significant bioactive molecules.However,efficient construction of this type of structure units is full of chal...
This work was supported by the National Natural Science Foundation of China(No.21871275).GAS thanks the Chinese Academy of Sciences for a Visiting Fellowship.
The 4,6-bis(arylimino)-1,2,3,7,8,9,10-heptahydrocyclohepta[b]quinoline-iron(II)chlorides(aryl=2,6-Me_(2)C_(6)H_(3) Fe1;2,6-Et_(2)C_(6)H_(3) Fe_(2);2,6-i-Pr_(2)C_(6)H_(3) Fe_(3);2,4,6-Me3C_(6)H_(2) Fe4;and 2,6-Et_(2)-4...
supported by the National Natural Science Foundation of China(21202186,21272199 and 21472213);the Croucher Foundation(Hong Kong)in the form of a CASCroucher Foundation Joint Laboratory Grant
The synthetic strategies towards tetraphenylene derivatives are comprehensively summarized in this review.Recent advances in the functionalized tetraphenylene skeleton for research into their structurally unique prope...
financial support from the National Basic Research Program of China(973 Project,No.2015CB856603);the National Natural Science Foundation of China(Nos.20472096,21372241,21361140350,20672127,21421091,21372250,21121062,21302203,20732008 and 21572052)
Nucleophilic chiral phosphine catalysis has been prosperous in asymmetric synthesis over the past two decades. Various tunable chiral phosphines display excellent activity and selectivity in asymmetric transformations...
Financial support from National Natural Science Foundation of China(No.21272237);the Ministry of Science and Technology of China(No.2011CB808600);the Chinese Academy of Sciences is gratefully acknowledged.
Although the NHC-catalyzed cyclization reactions have been well established for the synthesis of various heterocycles,the corresponding all carbon cyclization reaction for the synthesis of carbocycles is far less esta...
supported by the National Natural Science Foundation of China (20172032, 20872076);the Doctoral Program of Higher Education (200800030072)
Direct transformation of five-membered zirconacycles to carbocyclic compounds is of great synthetic interest.The reaction of zirconacycles with electrophiles containing at least two reactive functional groups or an ox...