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Cited 6 time in webofscience Cited 7 time in scopus
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Simple Synthetic Method for the Functionalized Benzo[c]cinnolines

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dc.contributor.authorLee, Da Seul-
dc.contributor.authorChatterjee, Tanmay-
dc.contributor.authorBan, Jaeyoung-
dc.contributor.authorRhee, Hakjune-
dc.contributor.authorCho, Eun Jin-
dc.date.available2019-01-22T14:08:06Z-
dc.date.issued2018-02-
dc.identifier.issn2365-6549-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/1183-
dc.description.abstractFunctionalized benzo[c]cinnoline derivatives were synthesized from easily accessible 2,2-diamino-1,1'-biaryls using a nitrite source. In this simple process, various functional groups were tolerated under mild reaction conditions, and the practicality of the process was demonstrated through the gram-scale production of the benzo[c]cinnolines.-
dc.format.extent4-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleSimple Synthetic Method for the Functionalized Benzo[c]cinnolines-
dc.typeArticle-
dc.identifier.doi10.1002/slct.201800278-
dc.identifier.bibliographicCitationCHEMISTRYSELECT, v.3, no.7, pp 2092 - 2095-
dc.description.isOpenAccessN-
dc.identifier.wosid000425627700021-
dc.identifier.scopusid2-s2.0-85042401432-
dc.citation.endPage2095-
dc.citation.number7-
dc.citation.startPage2092-
dc.citation.titleCHEMISTRYSELECT-
dc.citation.volume3-
dc.type.docTypeArticle-
dc.publisher.location독일-
dc.subject.keywordAuthorazo compounds-
dc.subject.keywordAuthorbenzo[c]cinnoline-
dc.subject.keywordAuthor2,2 '-diamino-1,1 '-biaryls-
dc.subject.keywordAuthornitrite-
dc.subject.keywordAuthornitrogen heterocycles-
dc.subject.keywordPlusAROMATIC NITRO COMPOUNDS-
dc.subject.keywordPlusCINNOLINE DERIVATIVES-
dc.subject.keywordPlusSELECTIVE FORMATION-
dc.subject.keywordPlusRADICAL CATIONS-
dc.subject.keywordPlusDIAZONIUM SALTS-
dc.subject.keywordPlusAZOXY COMPOUNDS-
dc.subject.keywordPlusREDUCTION-
dc.subject.keywordPlusLIGHT-
dc.subject.keywordPlus2,2'-DINITROBIPHENYL-
dc.subject.keywordPlusCYCLIZATION-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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