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Saikat, Maiti
유전체 항상성 연구단
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Reductive Ni-catalysis for stereoselective carboarylation of terminal aryl alkynes

DC Field Value Language
dc.contributor.authorSaikat Maiti-
dc.contributor.authorRhlee, Joon Ho-
dc.date.accessioned2021-11-16T04:50:00Z-
dc.date.available2021-11-16T04:50:00Z-
dc.date.created2021-11-01-
dc.date.issued2021-10-28-
dc.identifier.issn1359-7345-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/10681-
dc.description.abstractStereoselective 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.language영어-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleReductive Ni-catalysis for stereoselective carboarylation of terminal aryl alkynes-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000706768200001-
dc.identifier.scopusid2-s2.0-85118446763-
dc.identifier.rimsid76626-
dc.contributor.affiliatedAuthorSaikat Maiti-
dc.identifier.doi10.1039/d1cc04586e-
dc.identifier.bibliographicCitationCHEMICAL COMMUNICATIONS, v.57, no.86, pp.11346 - 11349-
dc.relation.isPartOfCHEMICAL COMMUNICATIONS-
dc.citation.titleCHEMICAL COMMUNICATIONS-
dc.citation.volume57-
dc.citation.number86-
dc.citation.startPage11346-
dc.citation.endPage11349-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusNICKEL CATALYSIS-
dc.subject.keywordPlus1,2-ADDITION-
dc.subject.keywordPlusIODIDES-
dc.subject.keywordPlusOLEFINS-
Appears in Collections:
Center for Genomic Integrity(유전체 항상성 연구단) > 1. Journal Papers (저널논문)
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