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dc.contributor.authorLee, YS-
dc.contributor.authorLee, JY-
dc.contributor.authorKim, DW-
dc.contributor.authorPark, HK-
dc.date.accessioned2024-01-21T15:37:22Z-
dc.date.available2024-01-21T15:37:22Z-
dc.date.created2021-09-05-
dc.date.issued1999-04-
dc.identifier.issn0040-4020-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/142254-
dc.description.abstractA chiral enamide 6, derived from L-malic acid, was converted to furo-indolizine 2 via N-acyliminium ion cyclization. Furo-indolizine 2 was transformed to indolizine derivatives 8 and 9 which have a substituent at angular position. (C) 1999 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleAsymmetric synthesis of furo[3,2-i]indolizines from L-malic acid-
dc.typeArticle-
dc.identifier.doi10.1016/S0040-4020(99)00158-1-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON, v.55, no.15, pp.4631 - 4636-
dc.citation.titleTETRAHEDRON-
dc.citation.volume55-
dc.citation.number15-
dc.citation.startPage4631-
dc.citation.endPage4636-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000079625500008-
dc.identifier.scopusid2-s2.0-0033537954-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusACYLIMINIUM ION CYCLIZATION-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusERYTHRINA-
dc.subject.keywordPlusALKALOIDS-
dc.subject.keywordPlusPYRROLIDINONES-
dc.subject.keywordPlusHETEROCYCLES-
dc.subject.keywordPlusENANTIOMERS-
dc.subject.keywordPlusROUTE-
dc.subject.keywordAuthorfuroindole-
dc.subject.keywordAuthorL-malic acid-
dc.subject.keywordAuthorN-acyliminium ion-
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