DSpace at KISTKIST ArticleOthers

Full metadata record

DC Field Value Language
dc.contributor.authorLEE, YS-
dc.contributor.authorKANG, DW-
dc.contributor.authorLEE, SJ-
dc.contributor.authorPARK, H-
dc.date.accessioned2024-01-21T20:17:18Z-
dc.date.available2024-01-21T20:17:18Z-
dc.date.created2022-01-10-
dc.date.issued1995-11-
dc.identifier.issn0022-3263-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/144916-
dc.description.abstractThe pyrrolidinoisoquinoline derivatives ((-)-3, (-)-4) and their antipodes ((+)-3, (+)-4) were prepared by reductive deoxygenation and reduction from the intermediates 9 and 10. The key intermediates 9 and 10 were prepared by a diastereoselective N-acyliminium ion cyclization of chiral lactams, which derived from L-malic acid and L-tartaric acid, respectively.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleASYMMETRIC-SYNTHESIS OF BOTH ENANTIOMERS OF PYRROLIDINOISOQUINOLINE DERIVATIVES FROM L-MALIC ACID AND L-TARTARIC ACID-
dc.typeArticle-
dc.identifier.doi10.1021/jo00127a019-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF ORGANIC CHEMISTRY, v.60, no.22, pp.7149 - 7152-
dc.citation.titleJOURNAL OF ORGANIC CHEMISTRY-
dc.citation.volume60-
dc.citation.number22-
dc.citation.startPage7149-
dc.citation.endPage7152-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1995TD63700019-
dc.identifier.scopusid2-s2.0-33751154800-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusENAMMONIUM IMINIUM REARRANGEMENT-
dc.subject.keywordPlusSTEREOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusDEOXYGENATION-
dc.subject.keywordPlusCYCLIZATIONS-
dc.subject.keywordPlusROUTE-
Appears in Collections:
KIST Article > Others
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML
Show Simple Item Record

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE