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dc.contributor.author조은진-
dc.date.accessioned2018-03-17T02:26:48Z-
dc.date.available2018-03-17T02:26:48Z-
dc.date.issued2012-02-
dc.identifier.citationTetrahedron, 2012, 68(8), P.2045-2051en_US
dc.identifier.issn0040-4020-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0040402012000166-
dc.description.abstractFacile and efficient procedures for the N-acylation reaction of amide derivatives with various acid anhydrides and the cyclization reaction of N-acylated amide derivatives with various hydrazine hydrochlorides were described. The reactions were carried out under microwave irradiation to give products in good yields in a few minutes. The synthesis of 1,3,5-trisubstituted-1,2,4-triazoles from benzamides can also be accomplished in a simple one-pot sequential reaction. (C) 2012 Elsevier Ltd. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherElsevier Science B.V., Amsterdam.en_US
dc.subjectMicrowave-assisted reactionen_US
dc.subject1,2,4-Triazoleen_US
dc.subjectN-Acylation reactionen_US
dc.subjectCyclization reactionen_US
dc.subjectOne-pot sequential reactionen_US
dc.subject1,2,4-TRIAZOLESen_US
dc.subjectCYCLIZATIONen_US
dc.subject1H-1,2,4-TRIAZOLESen_US
dc.subjectIMIDESen_US
dc.titleSynthesis of 1,3,5-trisubstituted-1,2,4-triazoles by microwave-assisted N-acylation of amide derivatives and the consecutive reaction with hydrazine hydrochloridesen_US
dc.typeArticleen_US
dc.relation.no8-
dc.relation.volume68-
dc.identifier.doi10.1016/j.tet.2012.01.003-
dc.relation.page2045-2051-
dc.relation.journalTETRAHEDRON-
dc.contributor.googleauthorLee, Jongbok-
dc.contributor.googleauthorHong, Myengchan-
dc.contributor.googleauthorJung, Yoonchul-
dc.contributor.googleauthorCho, Eun Jin-
dc.contributor.googleauthorRhee, Hakjune-
dc.relation.code2012209090-
dc.sector.campusS-
dc.sector.daehakGRADUATE SCHOOL[S]-
dc.sector.departmentDEPARTMENT OF BIONANOTECHNOLOGY-
dc.identifier.pidecho-
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GRADUATE SCHOOL[S](대학원) > BIONANOTECHNOLOGY(바이오나노학과) > Articles
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