supported by the National Key Research and Development Program of China(Grant Number 2021YFF0701-700);the Strategic Priority Research Program of the Chinese Academy of Sciences(XDB0590000).
The development of a nucleophilic fluorination protocol using hydrofluoric acid as the fluoride source represents a long-sought goal in the field of organofluorine chemistry.We report herein the realization of such a ...
A transition-metal-free strategy for the synthesis of tetrasubstituted furans is reported.Promoted by boron trifluo-ride diethyl etherate,the reaction of alkynyl sulfoxides with ynamides/ynol ethers proceeded via a ca...
Weare grateful for the financial support from the Natural Science Foundation of China(grant nos.21778009,21977010,and 22007033);National Key Research and Development Program“Synthetic Biology”Key Special Project of China(grant no.2018YFA0902504);China Postdoctoral Science Foundation(grant no.2021M690220);the Natural Science Foundation of Guangdong Province(grant nos.2020A1515010522,2020A1515010766,2019A1515110487,and 2019A151-5111184);the Foundation for Basic and Applied Research of Guangdong Province(grant no.2019A1515110489);and the Shenzhen Science and Technology Innovation Committee(grant nos.JCYJ20180507181527112,JCYJ-201805081522131455,and JCYJ20170817172023838).
Over the past 20 years,great efforts have been invested in developing site-specific approaches to protein modification to dissect protein functions directly and accurately.Here,we report a proximitytriggered group tra...
financial support from the National Key Research and Development Program"Synthetic Biology"Key Special Project of China (No. 2018YFA0902504);the China Postdoctoral Science Foundation (No. 2021M690220);the National Natural Science Foundation of China (Nos. 21778009 and21977010);the Natural Science Foundation of Guangdong Province(Nos. 2019A1515110487, 2020A1515010522 and 2019A1515111184);the Shenzhen Science and Technology Innovation Committee (Nos. JCYJ20180507181527112, JCYJ20180508152213145, and JCYJ20170817172023838);the Foundation for Basic and Applied Research of Guangdong Province (No. 2019A1515110489);Guangdong Medical Science Foundation (No. A2021413);financial support from Beijing National Laboratory of Molecular Science Open Grant (No. BNLMS20160112);Shenzhen-Hong Kong Institute of Brain Science-Shenzhen Fundamental Research Institutions (No. 2019SHIBS0004);supported by the high-performance computing platform of Peking University。
The modification and functionalization of peptides is of great significance in modern biotechnology and drug development. Here we report a highly reactive Michael-type warhead for the covalently modification of cystei...
Financial support from National Natural Science Foundation of China(Nos.21877043,21702068,21772050,22025102);the Fundamental Research Funds for the Central Universities,HUST(Nos.2019kfyXKJC080,2019JYCXJJ046);Huazhong University of Science and Technology are greatly appreciated。
A sulfonium ylide participated alkylation and arylation under transition-metal free conditions is described.The disparate reaction pattern allowed the separate activation of non-ylidic S-alkyl and S-aryl bond.Under ac...
financial support from the National Key Research and Development Program"Synthetic Biology"Key Special Project of China(No.2018YFA0902504);the Natural Science Foundation of China(Nos.21778009 and 21977010);the Natural Science Foundation ofGuangdongProvince(Nos.2020A1515010766,2020A1515010522,2019A1515111184 and 2019A1515110489);the Shenzhen Science and Technology Innovation Committee(Nos.JCYJ20180507181527112,JCYJ20180508152213145,and JCYJ20170817172023838);financial support from Beijing National Laboratory of Molecular Science Open Grant(No.BNLMS20160112);Shenzhen-Hong Kong Institute of Brain Science-Shenzhen Fundamental Research Institutions(No.2019SHIBS0004);supported by Proteomic Platform of Pingshan Translational Medicine Center;Shenzhen Bay Laboratory;the high-performance computing platform of Peking University.
Whilst most bioorthogonal reactions focus on targeting binding-site cysteine residues,proximity-induced reactivity effect ensures that reaction also occurs at nucleophilic lysine residues.We report one example here th...
the financial support from National Natural Science Foundation of China(Nos.21625206,21632009,21572258);the Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDB20000000).
The development of two highly reactive electrophilic trifluoromethylating reagents(trifluoromethyl)(4-nitrophenyl)bis(carbometh-oxy)methylide(1g)and(trifluoromethyl)(3-chlorophenyl)bis(carbomethoxy)methylide(1j)throug...
the support from the National Natural Science Foundation of China(No.21702013);the Fundamental Research Funds for the Central Universities(Nos.XK1802-6 and buctrc201721)at the BUCT.J;Tan and Y.Liu are thankful for the support from the Open Project Program(No.SPFW2019YB06)of Beijing Key Laboratory of Flavor Chemistry,Beijing Technology and Business University(BTBU)。
Sulfonium salts and sulfur ylides are important S(Ⅳ) motifs,and have displayed many unique reactivities to provide simple,effective,and often stereoselective synthesis toward sulfur containing compounds.Impressive de...
supported by the Science and Technology Foundation of Shenzhen, Shenzhen Science and Technology Innovation Committee (No. JCYJ20170818143001461)
A facile and highly efficient approach for selective O-difluoromethylation of 1,3-diones by recently developed bench-stable S-(difluoromethyl)sulfonium salt was described.And a broad range of difluoromthyl enol ethers...
The authors gratefully acknowledge the financial support from National Natural Science Foundation of China (Nos. 21625206, 21632009, 21572258, 21572259, 21421002, 21772098) and the Strategic Priority Research Program of the Chinese Academy of Sciences (No. XDB20000000) for financial support.