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Facile C–H arylation using catalytically active terminal sulfurs of 2 dimensional molybdenum disulfide

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dc.contributor.authorEunhee Hwang-
dc.contributor.authorSae Mi Lee-
dc.contributor.authorSora Bak-
dc.contributor.authorHee Min Hwang-
dc.contributor.authorHyunjung Kim-
dc.contributor.authorHyoyoung Lee-
dc.date.available2019-01-03T05:31:37Z-
dc.date.created2018-10-15-
dc.date.issued2018-10-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/5120-
dc.description.abstractThe first methodology of C–H arylation of heteroarene via 2D transition metal dichalcogenides that have catalytically active edge functional groups was described. The terminal sulfur groups could effectively catalyze a formation of an azo-linked intermediate with aryl diazonium salts, leading to produce heteroarenes with good yields. This novel methodology using bulk 2D transition metal dichalcogenides that have catalytically active edge functional groups can apply for various reactions to achieve C–C bond formation in the fields of heterogeneous catalysis that is easily separable, highly reusable, and inexpensive method. © 2018 Elsevier Lt-
dc.language영어-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectAryl (benzene) diazonium salts-
dc.subjectCross coupling-
dc.subjectC–H activation-
dc.subjectEdged sulfur-
dc.subjectMolybdenum disulfide-
dc.titleFacile C–H arylation using catalytically active terminal sulfurs of 2 dimensional molybdenum disulfide-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000448092800017-
dc.identifier.scopusid2-s2.0-85053909895-
dc.identifier.rimsid65781-
dc.contributor.affiliatedAuthorEunhee Hwang-
dc.contributor.affiliatedAuthorSae Mi Lee-
dc.contributor.affiliatedAuthorSora Bak-
dc.contributor.affiliatedAuthorHee Min Hwang-
dc.contributor.affiliatedAuthorHyunjung Kim-
dc.contributor.affiliatedAuthorHyoyoung Lee-
dc.identifier.doi10.1016/j.tetlet.2018.09.054-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.59, no.44, pp.3969 - 3973-
dc.relation.isPartOfTETRAHEDRON LETTERS-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume59-
dc.citation.number44-
dc.citation.startPage3969-
dc.citation.endPage3973-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusCROSS-COUPLING REACTIONS-
dc.subject.keywordPlusDIAZONIUM SALTS-
dc.subject.keywordPlusFREE-RADICALS-
dc.subject.keywordPlusMOS2-
dc.subject.keywordPlusFUNCTIONALIZATION-
dc.subject.keywordPlusTRANSISTOR-
dc.subject.keywordPlusCATALYSIS-
dc.subject.keywordPlusGRAPHENE-
dc.subject.keywordPlusDIOXIDE-
dc.subject.keywordPlusSPECTRA-
dc.subject.keywordAuthorAryl (benzene) diazonium salts-
dc.subject.keywordAuthorC-H activation-
dc.subject.keywordAuthorMolybdenum disulfide-
dc.subject.keywordAuthorCross coupling-
dc.subject.keywordAuthorEdged sulfur-
Appears in Collections:
Center for Integrated Nanostructure Physics(나노구조물리 연구단) > 1. Journal Papers (저널논문)
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