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dc.citation.endPage 11349 -
dc.citation.number 86 -
dc.citation.startPage 11346 -
dc.citation.title CHEMICAL COMMUNICATIONS -
dc.citation.volume 57 -
dc.contributor.author Maiti, Saikat -
dc.contributor.author Rhlee, Joon Ho -
dc.date.accessioned 2023-12-21T15:10:35Z -
dc.date.available 2023-12-21T15:10:35Z -
dc.date.created 2021-11-15 -
dc.date.issued 2021-10 -
dc.description.abstract Stereoselective dicarbofunctionalization of terminal aryl alkynes has been achieved through reductive Ni-catalysis. The exclusive regioselective and anti-addition selective alkylarylation of terminal alkynes is accomplished using alkyl iodide and aryl iodide as electrophilic coupling partners in the presence of NiBr2 as the catalyst and Mn as an inexpensive reductant. -
dc.identifier.bibliographicCitation CHEMICAL COMMUNICATIONS, v.57, no.86, pp.11346 - 11349 -
dc.identifier.doi 10.1039/d1cc04586e -
dc.identifier.issn 1359-7345 -
dc.identifier.scopusid 2-s2.0-85118446763 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/54816 -
dc.identifier.url https://pubs.rsc.org/en/content/articlelanding/2021/CC/D1CC04586E -
dc.identifier.wosid 000706768200001 -
dc.language 영어 -
dc.publisher ROYAL SOC CHEMISTRY -
dc.title Reductive Ni-catalysis for stereoselective carboarylation of terminal aryl alkynes -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Chemistry, Multidisciplinary -
dc.relation.journalResearchArea Chemistry -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus NICKEL CATALYSIS -
dc.subject.keywordPlus 1,2-ADDITION -
dc.subject.keywordPlus IODIDES -
dc.subject.keywordPlus OLEFINS -

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