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dc.contributor.authorKang, HY-
dc.contributor.authorHong, WS-
dc.contributor.authorLee, SH-
dc.contributor.authorChoi, KI-
dc.contributor.authorKoh, HY-
dc.date.accessioned2024-01-21T19:05:41Z-
dc.date.available2024-01-21T19:05:41Z-
dc.date.created2021-09-04-
dc.date.issued1997-01-
dc.identifier.issn0936-5214-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/144169-
dc.description.abstractThe reaction of hydrazones of 2,3-epoxycycloalkanone promoted by samarium(II) iodide has been investigated to study the behavior of the compounds containing C=N bonds in the presence of this powerful single-electron transfer reagent. For the hydrazones derived from 2,3-epoxycyclopentanone and 2,3-epoxycyclohexanone, 3-iodo-2-cycloalkenols were isolated while the corresponding 2-cycloalkenols were the products when the hydrazones from 2,3-epoxycycloheptanone and 2,3-epoxycyclooctanone were reacted.-
dc.languageEnglish-
dc.publisherGEORG THIEME VERLAG-
dc.subjectORGANIC-SYNTHESIS-
dc.subjectLANTHANIDES-
dc.subjectCYCLIZATION-
dc.subjectRADICALS-
dc.subjectIMINES-
dc.titleSamarium(II) iodide-promoted reactions of 2,3-epoxycycloalkanone hydrazones-
dc.typeArticle-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSYNLETT, no.1, pp.33 - +-
dc.citation.titleSYNLETT-
dc.citation.number1-
dc.citation.startPage33-
dc.citation.endPage+-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1997WF58500008-
dc.identifier.scopusid2-s2.0-0010406756-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusORGANIC-SYNTHESIS-
dc.subject.keywordPlusLANTHANIDES-
dc.subject.keywordPlusCYCLIZATION-
dc.subject.keywordPlusRADICALS-
dc.subject.keywordPlusIMINES-
dc.subject.keywordAuthorsamarium(II) iodide-
dc.subject.keywordAuthorhydrazones-
dc.subject.keywordAuthorepoxycycloalkanone-
dc.subject.keywordAuthorC=N bonds-
dc.subject.keywordAuthoriodination-
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