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College of Natural Sciences(자연과학대학)Dept. of Chemistry(화학과)CH-Journal Papers(저널논문)

Synthesis of 4-alkyl-1(2H)-phthalazinones and 4-alkyl-2,3-benzoxazin-1-ones via ring cleavage of 3-substituted N-alkylated-3-hydroxyisoindolin-1-ones

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dc.contributor.authorChun, TGko
dc.contributor.authorKim, KSko
dc.contributor.authorLee, Sko
dc.contributor.authorJeong, TSko
dc.contributor.authorLee, Hee Yoonko
dc.contributor.authorKim, YHko
dc.contributor.authorLee, WSko
dc.date.accessioned2013-03-04T13:49:10Z-
dc.date.available2013-03-04T13:49:10Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2004-04-
dc.identifier.citationSYNTHETIC COMMUNICATIONS, v.34, no.7, pp.1301 - 1308-
dc.identifier.issn0039-7911-
dc.identifier.urihttp://hdl.handle.net/10203/82838-
dc.description.abstractN-Alkyl (Me, Et, i-Pr, t-Bu)-substituted phthalimdes 5a-d were easily transformed to 1(2H)-phthalazinones 8d-i and 2,3-benzoxazin-1-ones 9d,f,and j via a one-pot addition-decyclization-cyclocondensation process.-
dc.languageEnglish-
dc.publisherTAYLOR & FRANCIS INC-
dc.subjectREGIOSELECTIVE SYNTHESIS-
dc.subjectCONVENIENT SYNTHESIS-
dc.subjectACID-
dc.subjectAGENTS-
dc.titleSynthesis of 4-alkyl-1(2H)-phthalazinones and 4-alkyl-2,3-benzoxazin-1-ones via ring cleavage of 3-substituted N-alkylated-3-hydroxyisoindolin-1-ones-
dc.typeArticle-
dc.identifier.wosid000220726600017-
dc.identifier.scopusid2-s2.0-1842481393-
dc.type.rimsART-
dc.citation.volume34-
dc.citation.issue7-
dc.citation.beginningpage1301-
dc.citation.endingpage1308-
dc.citation.publicationnameSYNTHETIC COMMUNICATIONS-
dc.identifier.doi10.1081/SCC-120030319-
dc.contributor.localauthorLee, Hee Yoon-
dc.contributor.nonIdAuthorChun, TG-
dc.contributor.nonIdAuthorKim, KS-
dc.contributor.nonIdAuthorLee, S-
dc.contributor.nonIdAuthorJeong, TS-
dc.contributor.nonIdAuthorKim, YH-
dc.contributor.nonIdAuthorLee, WS-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorheterocycles-
dc.subject.keywordAuthorN-alkyl-
dc.subject.keywordAuthorhydrazine-
dc.subject.keywordAuthorphthalimide-
dc.subject.keywordPlusREGIOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusCONVENIENT SYNTHESIS-
dc.subject.keywordPlusACID-
dc.subject.keywordPlusAGENTS-
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