supported by the National Natural Science Foundation of China(22271127,22071084);the Fundamental Research Funds for the Central Universities(lzujbky-2022-ey01)。
Reactions involving alkenyl acetates offer cost-effective and environmentally friendly routes for alkene synthesis,yet their asymmetric variant remains elusive.Concurrently,asymmetric conjugate alkenylation predominan...
the National Key R&D Program of China(No.2022YFA1302900 to H.Liu);National Natural Science Foundation of China(Nos.82130105,22337003,82121005 to H.Liu;and Nos.22177124,82322063 to J.Wang);Program of Shang-hai Academic Research Leader(No.23XD1460300 to J.Wang);the Lingang Laboratory(No.LG-GG-202204-02 to J.Wang)for supporting this work.We would like to acknowledge Shanghai Highline Therapeutics.
Heterocycle-braced cyclic peptides have demonstrated enhanced metabolic stability,increased potency and selectivity.Here,we present a rapid synthesis method for constructing Trp(C7)-alkene(E)-crosslinked cyclic peptid...
National Natural Science Foundation of China(Nos.22193011,21971120 and 21933008);National Science&Technology Fundamental Resource Investigation Program of China(No.2018FY201200)for financial support.
Catalytic enantioselective alkenylation is an efficient method to construct chiral alkene molecules,but the asymmetric alkenylation of simple alkenes catalyzed by metal-free catalysts remains an elusive challenge.Here...
supported by the National Natural Science Foundation of China(22001065);the Science and Technology Foundation of Hunan Province(2021JJ30090);Guangdong Provincial Key Laboratory of Catalysis(2020B121201002);Shenzhen Science and Technology Program(KQTD20210811090112004);supported by Center for Computational Science and Engineering at SUSTech;the CHEM high-performance supercomputer cluster(CHEM-HPC)located at the Department of Chemistry,SUSTech。
The conversion of commercially available chiral sulfinamides into pharmaceutically useful chiral sulfoximines via direct SIVfunctionalization is synthetically attractive but challenging due to the competitive reaction...
suported by the National Natural Science Foundation of China (2187,1117, 91956203);the “111” Program of Minister of Education, Beijing National Laboratory for Molecular Sciences (BNLMS202109);the Science and Technology Commission of Shanghai Municipality (19JC1430100)。
Catalyst innovation lies at the heart of transition-metal-catalyzed reaction development. In this article, we have explored the C(sp2)–H alkenylation activity with novel spirocyclic N-heterocyclic carbene(NHC)-based ...
the National Natural Science Foundation of China(Nos.82130105,82103969 and 82273766);SA-SIBS Scholarship Program,the Youth Innovation Promotion Association CAS(2020282);grant from Lingang Laboratory(LG202103-02-06).
Comprehensive Summary Herein,we have developed a strategy of Rh(III)-catalyzed C—H activation of N-nitrosoanilines and iodonium ylides to construct novel tetralydrocarbzol-4-one scaffolds,which provided valuable temp...
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...
The project is supported by NSFC(91956104),BNLMS,and Laboratory for Synthetic Chemistry and Chemical Biology of Health@InnoHK of ITC,HKSAR.
The chemistry of alkoxy radicals was extensively explored during the period of 1960s to 1990s,but it has remained dormant for the past few decades.Recently,alkoxy radicals attract the attentions again,because new meth...
support from the National Natural Science Foundation of China(No.21772185);supported by the Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDB20000000).
An efficient asymmetric alkenylation between 3-vinylindoles and isatin derivatives was developed under catalysis of a chiral copper complex.A series of optically active 3-alkenyl-3-substituted oxindoles were obtained ...
the financial support from the National Natural Science Foundation of China(grant nos.91856111,21871288,21690074,and 21821002);the Strategic Priority Research Program of the Chinese Academy of Sciences(grant no.XDB 20000000).
Herein,we report the first highly enantioselective Ni-catalyzed arylation and alkenylation of simple aldehydes using readily available and stable organoboronic esters.This protocol provides various chiral secondary al...