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dc.contributor.author이학준-
dc.date.accessioned2018-03-20T06:24:03Z-
dc.date.available2018-03-20T06:24:03Z-
dc.date.issued2014-05-
dc.identifier.citationJOURNAL OF ORGANIC CHEMISTRY, 권: 79, 호: 9, 페이지: 4206-4211en_US
dc.identifier.issn0022-3263-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/jo500462n-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/49638-
dc.description.abstractThe palladium-catalyzed coupling of N,N-ditosylbenzylamines with arylboronic acids has been investigated, and the resulting diarylmethanes were obtained in high yields. Conversion of the amine to a N,N-ditosylimide group provided an efficient leaving group for the Pd-catalyzed benzylation of arylboronic acids.en_US
dc.description.sponsorshipThis research was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF-2012R1A1A2001005). S.Y. acknowledges financial support from the Korean Ministry of Education through the BK21-Plus project for the Hanyang University graduate program. We acknowledge Mr. Y. Lee, Mr. J. Baek, and Miss Y. Lee for helping to obtain spectral data and the Daegu Center of KBSI for obtaining HRMS data.en_US
dc.language.isoenen_US
dc.publisherAMER CHEMICAL SOC, 1155 16TH ST, NW, WASHINGTON, DC 20036 USAen_US
dc.subjectCROSS-COUPLING REACTIONSen_US
dc.titlePalladium-Catalyzed Benzylation of Arylboronic Acids with N,N-Ditosylbenzylaminesen_US
dc.typeArticleen_US
dc.relation.volume79-
dc.identifier.doi10.1021/jo500462n-
dc.relation.page4206-4211-
dc.relation.journalJOURNAL OF ORGANIC CHEMISTRY-
dc.contributor.googleauthorYoon, Sangeun-
dc.contributor.googleauthorHong, Myeng Chan-
dc.contributor.googleauthorRhee, Hakjune-
dc.relation.code2014034092-
dc.sector.campusS-
dc.sector.daehakGRADUATE SCHOOL[S]-
dc.sector.departmentDEPARTMENT OF BIONANOTECHNOLOGY-
dc.identifier.pidhrhee-
dc.identifier.researcherIDO-5765-2017-
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