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dc.contributor.authorLee, SG-
dc.contributor.authorLim, CW-
dc.contributor.authorSong, CE-
dc.contributor.authorPark, DH-
dc.date.accessioned2024-01-21T20:12:12Z-
dc.date.available2024-01-21T20:12:12Z-
dc.date.created2022-01-10-
dc.date.issued1996-01-
dc.identifier.issn0039-7911-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/144834-
dc.description.abstractOzonolyses of ethyl indole-2-carboxylate (1a) and ethyl 1-methylindole-2-carboxylate (1b) in participating solvent, methanol, afforded alpha-methoxyhydroperoxides 7a and 7b in 90% and 89% yields, respectively, which are the first isolated solvent-trapped carbonyl oxides from ozonolysis of indole derivatives.-
dc.languageEnglish-
dc.publisherMARCEL DEKKER INC-
dc.subjectVINYL ETHERS-
dc.titleFormation of stable solvent-trapped carbonyl oxides from the ozonolysis of indole derivatives-
dc.typeArticle-
dc.identifier.doi10.1080/00397919608004787-
dc.description.journalClass1-
dc.identifier.bibliographicCitationSYNTHETIC COMMUNICATIONS, v.26, no.24, pp.4623 - 4631-
dc.citation.titleSYNTHETIC COMMUNICATIONS-
dc.citation.volume26-
dc.citation.number24-
dc.citation.startPage4623-
dc.citation.endPage4631-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1996VX72900013-
dc.identifier.scopusid2-s2.0-0030471804-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusVINYL ETHERS-
dc.subject.keywordAuthorcarbonyl oxide-
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