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dc.contributor.authorKim, JH-
dc.contributor.authorLee, YS-
dc.contributor.authorKim, CS-
dc.date.accessioned2024-01-21T16:33:20Z-
dc.date.available2024-01-21T16:33:20Z-
dc.date.created2021-09-03-
dc.date.issued1998-11-01-
dc.identifier.issn0385-5414-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/142744-
dc.description.abstractSyntheses of praziquantel have been accomplished via an N-acyliminium ion by several routes including the tandem nucleophilic addition-cyclization sequence from amido acetal (8) or (10) and a stepwise cyclization of enamide (9) generated from the nucleophilic addition reaction of amido acetal (8) or (10).-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectASYMMETRIC-SYNTHESIS-
dc.subject(+/-)-3-DEMETHOXYERYTHRATIDINONE-
dc.titleSynthesis of praziquantel via N-acyliminium ion cyclization of amido acetals through several synthetic routes-
dc.typeArticle-
dc.description.journalClass1-
dc.identifier.bibliographicCitationHETEROCYCLES, v.48, no.11, pp.2279 - 2285-
dc.citation.titleHETEROCYCLES-
dc.citation.volume48-
dc.citation.number11-
dc.citation.startPage2279-
dc.citation.endPage2285-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000077403000007-
dc.identifier.scopusid2-s2.0-0001583427-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusASYMMETRIC-SYNTHESIS-
dc.subject.keywordPlus(+/-)-3-DEMETHOXYERYTHRATIDINONE-
dc.subject.keywordAuthorpraziquantel-
dc.subject.keywordAuthorN-acyliminium ion-
dc.subject.keywordAuthorAmidoacetal-
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