Repository at Hanyang UniversityCOLLEGE OF NATURAL SCIENCES[S](자연과학대학)CHEMISTRY(화학과)Articles
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dc.contributor.author조천규-
dc.date.accessioned2022-05-04T00:55:48Z-
dc.date.available2022-05-04T00:55:48Z-
dc.date.issued2020-09-
dc.identifier.citationORGANIC LETTERS, v. 22, no. 19, page. 7588-7593en_US
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acs.orglett.0c02785-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/170555-
dc.description.abstractImidazole-selective intermolecular hydroamination reaction has been discovered. This unprecedented additive-free addition reaction proceeds in an exclusively regioselective and stereoselective manner with high atom economy under extremely mild reaction conditions.en_US
dc.description.sponsorshipWe gratefully acknowledge financial support from the National Research Foundation of Korea (No. 2014R1A5A1011165).en_US
dc.language.isoenen_US
dc.publisherAMER CHEMICAL SOCen_US
dc.subjectDEFICIENT 1,3-CONJUGATED ENYNESen_US
dc.subjectSTEREOSELECTIVE HYDROAMINATIONen_US
dc.subjectCATALYZED HYDROAMINATIONen_US
dc.subjectALKENESen_US
dc.subjectACCESSen_US
dc.subject2,3-DIHYDROISOXAZOLESen_US
dc.subjectCYCLOADDITIONen_US
dc.subjectCONSTRUCTIONen_US
dc.subjectDERIVATIVESen_US
dc.titleImidazole-Selective Alkyne Hydroamination under Physiological Conditionsen_US
dc.typeArticleen_US
dc.relation.no19-
dc.relation.volume22-
dc.identifier.doi10.1021/acs.orglett.0c02785-
dc.relation.page7588-7593-
dc.relation.journalORGANIC LETTERS-
dc.contributor.googleauthorKang, Hyung-Joon-
dc.contributor.googleauthorLee, Joon-Ho-
dc.contributor.googleauthorKim, Dong-Hyun-
dc.contributor.googleauthorCho, Cheon-Gyu-
dc.relation.code2020048882-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF NATURAL SCIENCES[S]-
dc.sector.departmentDEPARTMENT OF CHEMISTRY-
dc.identifier.pidccho-
dc.identifier.orcidhttps://orcid.org/0000-0003-4851-5671-
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