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dc.contributor.authorLEE, YS-
dc.contributor.authorKANG, DW-
dc.contributor.authorLEE, SJ-
dc.contributor.authorPARK, H-
dc.date.accessioned2024-01-21T21:14:19Z-
dc.date.available2024-01-21T21:14:19Z-
dc.date.created2021-09-02-
dc.date.issued1995-01-
dc.identifier.issn0039-7911-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/145420-
dc.description.abstractStudies on the stereoselective synthesis of a pyrrolidinoisoquinoline derivative using acyliminium ion cyclization of hydroxylactams are described. Cyclization reaction of chiral hydroxylactams 2a similar to c, derived from (L)-tartaric acid and phenethylamine, afforded one diastereomer 3 under a variety of acidic conditions in moderate to good yields.-
dc.languageEnglish-
dc.publisherMARCEL DEKKER INC-
dc.titleSTEREOSELECTIVE SYNTHESIS OF AN ISOQUINOLINOPYRROLIDINONE BY ACYLIMINIUM ION CYCLIZATION OF CHIRAL HYDROXYLACTAMS-
dc.typeArticle-
dc.identifier.doi10.1080/00397919508015871-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSYNTHETIC COMMUNICATIONS, v.25, no.13, pp.1947 - 1956-
dc.citation.titleSYNTHETIC COMMUNICATIONS-
dc.citation.volume25-
dc.citation.number13-
dc.citation.startPage1947-
dc.citation.endPage1956-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1995QY01200008-
dc.identifier.scopusid2-s2.0-0029073897-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusENAMMONIUM IMINIUM REARRANGEMENT-
dc.subject.keywordPlusPYRROLOISOQUINOLINE ANTIDEPRESSANTS-
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