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dc.contributor.author윤소원-
dc.date.accessioned2016-06-08T06:55:21Z-
dc.date.available2016-06-08T06:55:21Z-
dc.date.issued2015-01-
dc.identifier.citationADVANCED SYNTHESIS and CATALYSIS, v. 357, NO 1, Page. 227-234en_US
dc.identifier.issn1615-4169-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/21592-
dc.identifier.urihttp://onlinelibrary.wiley.com/doi/10.1002/adsc.201400759/full-
dc.description.abstractA highly effective silver(I)-mediated C-H amination of 2-alkenylanilines has been developed to afford a diverse range of substituted indoles. High functional group tolerance, broad substrate scope, simple/fast/high-yielding reaction, and recovery/reuse of the inexpensive silver oxidant are noteworthy. Furthermore, an uncommon migratory process of beta-monosubstituted 2-alkenylanilines with solvent-dependence was demonstrated.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 Ministry of Education and MSIP (Nos. 2012R1A1A2041471, 2012M3A7B4049654, and 2014-011165).-
dc.language.isoenen_US
dc.publisherWILEY-V C H VERLAG GMBHen_US
dc.subjectcyclizationen_US
dc.subjectindolesen_US
dc.subjectmigrationen_US
dc.subjectoxidationen_US
dc.subjectsilveren_US
dc.titleSilver(I)-Mediated C-H Amination of 2-Alkenylanilines: Unique Solvent-Dependent Migratory Aptitudeen_US
dc.typeArticleen_US
dc.relation.no1-
dc.relation.volume357-
dc.identifier.doi10.1002/adsc.201400759-
dc.relation.page227-234-
dc.relation.journalADVANCED SYNTHESIS & CATALYSIS-
dc.contributor.googleauthorYoun, So Won-
dc.contributor.googleauthorKo, Tae Yun-
dc.contributor.googleauthorJang, Min Jung-
dc.contributor.googleauthorJang, Su San-
dc.relation.code2015002749-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF NATURAL SCIENCES[S]-
dc.sector.departmentDEPARTMENT OF CHEMISTRY-
dc.identifier.pidsowony73-
Appears in Collections:
COLLEGE OF NATURAL SCIENCES[S](자연과학대학) > CHEMISTRY(화학과) > Articles
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