DICP OpenIR
Subject Area物理化学
Lewis Acid-Catalyzed, Copper(II)-Mediated Synthesis of Heteroaryl Thioethers under Base-Free Conditions
Dai, Chao1,2; Xu, Zhaoqing1; Huang, Fei1; Yu, Zhengkun1; Gao, Yan-Feng2; Xu ZQ(许兆青); Yu ZK(余正坤); YanFengGao
Source PublicationJOURNAL OF ORGANIC CHEMISTRY
2012-05-04
DOI10.1021/jo202624s
Volume77Issue:9Pages:4414-4419
Indexed BySCI ; IC ; CCR
SubtypeArticle
Department2
Funding Project203
Contribution Rank1,1
WOS HeadingsScience & Technology ; Physical Sciences
WOS SubjectChemistry, Organic
WOS Research AreaChemistry
WOS KeywordPHASE TRANSFER CATALYSIS ; DIRECT ARYLATION ; BIOLOGICAL-ACTIVITIES ; S-ALKYLATION ; FUNCTIONALIZATIONS ; DECOMPOSITION ; HETEROCYCLES ; BENZOXAZOLE ; DERIVATIVES ; DISULFIDES
AbstractA Lewis acid (Ag-I, Ni-II, or Fe-II) catalyzed, Cu-II-mediated thiolation reaction between heteroarenes and thiols was achieved with good yield under base-free conditions. DMSO could serve as an effective methylthiolation reagent for the synthesis of heterocyclic methyl thioethers.
Language英语
WOS IDWOS:000303492300023
Citation statistics
Cited Times:118[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://cas-ir.dicp.ac.cn/handle/321008/118408
Collection中国科学院大连化学物理研究所
Corresponding AuthorXu ZQ(许兆青); Yu ZK(余正坤); YanFengGao
Affiliation1.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
2.Zhengzhou Univ, Dept Bioengn, Zhengzhou 450001, Peoples R China
Recommended Citation
GB/T 7714
Dai, Chao,Xu, Zhaoqing,Huang, Fei,et al. Lewis Acid-Catalyzed, Copper(II)-Mediated Synthesis of Heteroaryl Thioethers under Base-Free Conditions[J]. JOURNAL OF ORGANIC CHEMISTRY,2012,77(9):4414-4419.
APA Dai, Chao.,Xu, Zhaoqing.,Huang, Fei.,Yu, Zhengkun.,Gao, Yan-Feng.,...&YanFengGao.(2012).Lewis Acid-Catalyzed, Copper(II)-Mediated Synthesis of Heteroaryl Thioethers under Base-Free Conditions.JOURNAL OF ORGANIC CHEMISTRY,77(9),4414-4419.
MLA Dai, Chao,et al."Lewis Acid-Catalyzed, Copper(II)-Mediated Synthesis of Heteroaryl Thioethers under Base-Free Conditions".JOURNAL OF ORGANIC CHEMISTRY 77.9(2012):4414-4419.
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