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dc.contributor.author윤소원-
dc.date.accessioned2019-11-26T05:52:56Z-
dc.date.available2019-11-26T05:52:56Z-
dc.date.issued2017-06-
dc.identifier.citationANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v. 56, no. 23, page. 6636-6640en_US
dc.identifier.issn1433-7851-
dc.identifier.issn1521-3773-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201702205-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/114629-
dc.description.abstractA Pd-catalyzed intermolecular oxidative annulation between N-Ts-anilines and styrenes was developed. This method offers a straightforward and robust approach to a wide range of 3-arylindoles using readily available starting materials with good functional-group tolerance and high regioselectivity and efficiency. Further elaboration of the products obtained from this process provided access to highly functionalized and structurally diverse indoles, for example, 3-(indol-3-yl)carbazoles, 1,9-dihydropyrrolo-[2,3-b]carbazoles, and 3'-aryl-3,5'-biindoles.en_US
dc.description.sponsorshipThis work was supported by both Basic Science Research Program and Nano.Material Technology Department Program through the National Research Foundation of Korea (NRF) funded by the Korea government (MSIP) (Nos. 2012M3A7B4049644, 2015R1A2A2A01002559, and 2014-011165).en_US
dc.language.isoen_USen_US
dc.publisherWILEY-V C H VERLAG GMBHen_US
dc.subjectC-H activationen_US
dc.subjecthomogeneous catalysisen_US
dc.subjectindolesen_US
dc.subjectpalladiumen_US
dc.subjectregioselectivityen_US
dc.titlePalladium-Catalyzed Regioselective Synthesis of 3-Arylindoles from N-Ts-Anilines and Styrenesen_US
dc.typeArticleen_US
dc.relation.no23-
dc.relation.volume56-
dc.identifier.doi10.1002/anie.201702205-
dc.relation.page6636-6640-
dc.relation.journalANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.contributor.googleauthorYoun, So Won-
dc.contributor.googleauthorKo, Tae Yun-
dc.contributor.googleauthorJang, Young Ho-
dc.relation.code2017003492-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF NATURAL SCIENCES[S]-
dc.sector.departmentDEPARTMENT OF CHEMISTRY-
dc.identifier.pidsowony73-
dc.identifier.researcherIDP-2060-2015-
dc.identifier.orcidhttp://orcid.org/0000-0002-2134-6487-
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COLLEGE OF NATURAL SCIENCES[S](자연과학대학) > CHEMISTRY(화학과) > Articles
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