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dc.contributor.author오창호-
dc.date.accessioned2016-06-09T08:18:18Z-
dc.date.available2016-06-09T08:18:18Z-
dc.date.issued2015-01-
dc.identifier.citationSYNTHETIC COMMUNICATIONS, v. 45, NO 6, Page. 758-776en_US
dc.identifier.issn0039-7911-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/21641-
dc.identifier.urihttp://www.tandfonline.com/doi/full/10.1080/00397911.2014.987353?scroll=top&needAccess=true-
dc.description.abstractA simple method to synthesize N-heteropolycyclic quinazolinones was developed including Knoevenagel condensation of quinazolines and aldehydes and Friedel-Craft alkylation as key steps. Knoevenagel reaction of 2-methyl-3-phenylquinazolin-4(3H)-one proceeded smoothly under a basic condition and subsequent Friedel-Craft alkylation with BrOnsted acid gave the N-heteropolycyclic quinazolinones in good yields. Furthermore, these new polycyclic compounds were converted into organic molecules having a long -conjugation system by treatment of 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) to utilize them as organic dyes.en_US
dc.language.isoenen_US
dc.publisherTAYLOR & FRANCIS INCen_US
dc.subjectFriedel–Crafts alkylationen_US
dc.subjectKnoevenagel condensationen_US
dc.subjectN-heteropolycycleen_US
dc.subjectquinazolinoneen_US
dc.titleSYNTHESIS OF N-HETEROPOLYCYCLIC COMPOUNDS INCLUDING QUINAZOLINONE SKELETON USING FRIEDEL-CRAFTS ALKYLATIONen_US
dc.typeArticleen_US
dc.relation.no6-
dc.relation.volume45-
dc.identifier.doi10.1080/00397911.2014.987353-
dc.relation.page768-776-
dc.relation.journalSYNTHETIC COMMUNICATIONS-
dc.contributor.googleauthorOh, Bu Keun-
dc.contributor.googleauthorKo, Eun Bi-
dc.contributor.googleauthorHan, Jin Wook-
dc.contributor.googleauthorOh, Chang Ho-
dc.relation.code2015000933-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF NATURAL SCIENCES[S]-
dc.sector.departmentDEPARTMENT OF CHEMISTRY-
dc.identifier.pidchangho-
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COLLEGE OF NATURAL SCIENCES[S](자연과학대학) > CHEMISTRY(화학과) > Articles
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