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dc.contributor.author이학준-
dc.date.accessioned2023-07-20T01:24:53Z-
dc.date.available2023-07-20T01:24:53Z-
dc.date.issued2018-04-
dc.identifier.citationJournal of Organic Chemistry, v. 83, NO. 8, Page. 4805-4811-
dc.identifier.issn0022-3263;1520-6904-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acs.joc.8b00022en_US
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/183959-
dc.description.abstractThe copper(I)-catalyzed azide-alkyne cycloaddition reaction has been extensively studied and widely applied in organic synthesis. However, the formation of 1,2,3-triazoles with electron-deficient azide has been a challenging problem. In this report, we have demonstrated the formation of regioselective 1,4-disubstituted 1,2,3-triazoles from various types of aryl terminal alkynes and azidoformates, which are electron-deficient azides, using a commercialized [Cu-(CH3CN)(4)]PF6 copper(I) catalyst under mild conditions.-
dc.description.sponsorshipThis research was supported by the Basic Science Research Program administered through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (2015R1D1A1A09058536) and by the Korean Ministry of Education through the BK21-Plus Project of the Hanyang University Graduate Program.-
dc.languageen-
dc.publisherAmerican Chemical Society-
dc.titleCopper(I)-Catalyzed Synthesis of 1,4-Disubstituted 1,2,3-Triazoles from Azidoformates and Aryl Terminal Alkynes-
dc.typeArticle-
dc.relation.no8-
dc.relation.volume83-
dc.identifier.doi10.1021/acs.joc.8b00022-
dc.relation.page4805-4811-
dc.relation.journalJournal of Organic Chemistry-
dc.contributor.googleauthorLee, Heejin-
dc.contributor.googleauthorLee, Jae Kyun-
dc.contributor.googleauthorMin, Sun-Joon-
dc.contributor.googleauthorSeo, Hyeonglim-
dc.contributor.googleauthorLee, Youngbok-
dc.contributor.googleauthorRhee, Hakjune-
dc.sector.campusE-
dc.sector.daehak과학기술융합대학-
dc.sector.department화학분자공학과-
dc.identifier.pidhrhee-


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