相关期刊:《Journal of Wuhan University of Technology(Materials Science)》《International Journal of Organic Chemistry》《Green Synthesis and Catalysis》《Journal of Chinese Pharmaceutical Sciences》更多>>
相关基金:国家自然科学基金Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry浙江省杰出青年科学基金中国博士后科学基金更多>>
the National Natural Science Foundation of China(No.22271245);the Jiangxi Province Science and Technology Project(Nos.20212AEI91002 and 20202ACBL213002);the Open Research Fund of School of Chemistry and Chemical Engineering,Henan Normal University(No.2021ZD01)for financial support.
A new cooperative nickel reductive catalysis and N,N-dimethylformamide-mediated strategy for umpolung C–S radical reductive cross coupling of S-(trifluoromethyl)arylsulfonothioates with alkyl halides to produce alkyl...
This work was financially supported by the National Natural Science Foundation of China(Nos.22011540002 and 22131005);Xiaomi Young Scholar Program,the Fundamental Research Funds for the Central Universities,the Advanced Talents Incubation Program of Hebei University,and University of Science and Technology Beijing and Hebei University are gratefully acknowledged.
The development of heterogeneous molecule-based catalysts for red light-mediated photocatalysis is still challenging due to the improper light absorption for most materials and the photoactivity deactivation for solid...
support from the National Natural Science Foundation of China(NSFC,No.21702019)and Advanced Catalysis and Green Manufacturing Collaborative Innovation Center,Changzhou University;Haibo Ge,Mazen Elsaid and Chong Liu acknowledge NSF(No.CHE-2029932),Robert A.Welch Foundation(No.D-2034-20200401),and the Texas Tech University for financial support.
Thioether skeletons are widely present in drugs,natural products,functional materials,and life science.In the past decade,the selective C–H functionalization of thioethers has been extensively studied to construct no...
Funded by the National Natural Science Foundation of China(No.21571144)
An efficient, practical, highly selective and environmentally benign method is reported for the synthesis of aryl thioethers via the coupling of thiols with aryl boronic acids in the presence of NaOH and a catalytic a...
Some new asymmetric thioethers 5 and 4-thiazolidinones 6 have been obtained from condensation of 5-formyl-3-(pyridin-4'-yl)-1,2,4-triazino[5,6-b] indole (3) with halogenated aromatic amines followed by addition of thi...
Acknowledgement This work was supported by National Natural Science Foundation of China (No. 21072030), Research Fund for the Doctoral Program of Higher Education of China (No. 20123514110003), the Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry (No. 2012-1707), and Fuzhou University (Nos. 022318, 022494).
A facile preparation of allylic trifluoromethyl thioethers was achieved by using a copper reagent. The reaction of (bpy)Cu(SCF3) with various allylic bromides afforded the desired trifluoromethylthiolation product...
the National Natural Science Foundation of China(No.20902070);Natural Science Foundation of Zhejiang Province(No.Y4100579);Qianjiang Talents Program of Zhejiang Province(No.QJD0902004) for financial supports
Tetrabutylammonium fluoride (TBAF) effectively facilitated a denitrative substitution reaction of electron-deficient nitroarenes with phenylthiotrimethylsilane (PhSTMS) under mild and base-free neutral conditions ...
This work was supported by the National Natural Science Foundation of China (No. 20572013) and the Doctoral Foundation of Anshan Normal University.
Using 2-[bis(alkylthio)methylene]-3-oxo-N-o-tolylbutanamides 1 as odorless thiol equivalents, an efficient and odorless synthesis of thioethers has been developed. Promoted by NaOH in EtOH, the cleavage of 1 commenc...
Natural Science Foundation of China (Grant No.20672009);the Major State Basic Research Development Program(Grant No.2004CB719900).
An efficient and environmental-friendly one-pot procedure has been developed for the synthesis of 1,3,4-oxadiazole-5- thioethers by the reaction of acylhydrazine with carbon disulfide and organic halides or α, β-uns...
The disulfides reacted with zinc in DMF, followed by alkyl halides, giving unsymmetrical thioether in excellent yields. This reaction takes place under mild and neutral conditions.