293 0

Full metadata record

DC FieldValueLanguage
dc.contributor.author이학준-
dc.date.accessioned2021-07-22T05:24:54Z-
dc.date.available2021-07-22T05:24:54Z-
dc.date.issued2020-03-
dc.identifier.citationSYNTHESIS-STUTTGART, v. 52, no. 6, page. 917-927en_US
dc.identifier.issn1437-210X-
dc.identifier.issn0039-7881-
dc.identifier.urihttps://www.thieme-connect.de/products/ejournals/abstract/10.1055/s-0039-1690759-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/163085-
dc.description.abstractWe synthesized various carbazoles from anilines through a three-step process with good overall yields (up to 48%). This process comprises N-acetylation, copper(0)-mediated Ullmann homocoupling, and acid-mediated intramolecular amination. It permits various functional groups on the substrate. Scale-up of the developed threestep synthetic route to carbazoles was also demonstrated.en_US
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 (2018R1D1A1A09082498) and by the Korean Ministry of Education through the BK21-Plus Project of the Hanyang University Graduate Program.en_US
dc.language.isoen_USen_US
dc.publisherGEORG THIEME VERLAG KGen_US
dc.subjectN-acetylationen_US
dc.subjectaryl homocouplingen_US
dc.subjectUllmann coupling reactionen_US
dc.subjectTäuber carbazole synthesisen_US
dc.subjectintramolecular aminationen_US
dc.titleSite-Specific Synthesis of Carbazole Derivatives through Aryl Homocoupling and Aminationen_US
dc.typeArticleen_US
dc.relation.no6-
dc.identifier.doi10.1055/s-0039-1690759-
dc.relation.page917-927-
dc.relation.journalSYNTHESIS-STUTTGART-
dc.contributor.googleauthorBan, J.-
dc.contributor.googleauthorLim, M.-
dc.contributor.googleauthorBaek, J.-
dc.contributor.googleauthorRhee, H.-
dc.contributor.googleauthorShabbir, S.-
dc.relation.code2020053901-
dc.sector.campusE-
dc.sector.daehakCOLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY[E]-
dc.sector.departmentDEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING-
dc.identifier.pidhrhee-


qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE