the NSFC(Nos.22071098,21931002 and 22101123);the Guangdong Provincial Key Laboratory of Catalysis(No.2020B121201002);the Shenzhen Science and Technology Innovation Committee(No.JCYJ20200109140812302);Introduction of Major Talent Projects in Guangdong Province(No.2019CX01C079);Outstanding Talents Training Fund in Shenzhen,for their financial support.
Metallacyclopentadienes are important metallacycles and regarded as intermediates in many reactions,therefore,new methods to achieve them are anticipated.In this study,a formal[3+2]method,through the reactions of an o...
The authors are grateful for the financial support provided by the National Natural Science Foundation of China (Nos. 21672176 and 21332007);the National Key R&D Pregram of China (No. 2017YFA0207302).
In recent years,exciting progress has been made in the field of direct transformation of amides,nevertheless,the condensation between two amides remains rare and restricted to homo-coupling reactions.Herein,we report ...
support provided by the National Key R&D Program of China (No.2017YFA0207302);the National Natural Science Foundation of China (Nos.21672176 and 21332007).
Summary of main observation and conclusion Direct functionalization of alkenes and direct transformation of carboxamides are two exciting areas that have attracted considerable attention in recent years.We report here...
Project supported by the National Basic Research Program of China (973 Program) (No. 2010CB833200), the National Natural Science Foundation of China (Nos. 21172247, 21032002, 20921091, 20672129, 20621062, 20772143) and the Chinese Academy of Sciences ("Knowledge Innovation", KJCX2.YW.H08).
Through the chiral-pool based synthesis of both enantiomers of schweinfurthinol, it has been proven that this natural product isolated from the seeds of Canarium schweinfurthii possesses an (S) configuration. The op...
Supported by the National Science Fund for Distinguished Young Investigators; the NNSF ofChina (20272048; 203900505); the Ministry of Education (Key Project 104201); and the Specialized Research Fundfor the Doctoral Program of Higher Education (20020384004)
Project (No. 29672042, 29832050) supported by the National Natural Science Foundation of China.
Structural effect of substituents directly bonded to carbanions bearing a phosphorate moiety is examined. Nucleophihc addition of phosphonate carbanion to 1-nitroalkene followed by subsequent reaction with chlorotrim...
Project supported by the National Natural Science Foundation of China
Halophilic attacks on C-X bonds (X=Br,Cl) by a base can easily initiate mtermolecular bromme-chlonne exchange reactions either among bromine-or chlorine-containing perhaloalkane molecules of different compounds of amo...
The reactions of α-(alkoxysilyl)allyl anions 4 with electrophiles were studied. α-Alkylation with alkyl halides was favoured, whereas γ-selection was achieved in the reaction with aldehydes.