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dc.contributor.authorKang, KH-
dc.contributor.authorPae, AN-
dc.contributor.authorChoi, KI-
dc.contributor.authorCho, YS-
dc.contributor.authorChung, BY-
dc.contributor.authorLee, JE-
dc.contributor.authorJung, SH-
dc.contributor.authorKoh, HY-
dc.contributor.authorLee, HY-
dc.date.accessioned2024-01-21T12:43:26Z-
dc.date.available2024-01-21T12:43:26Z-
dc.date.created2021-09-05-
dc.date.issued2001-02-05-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/140711-
dc.description.abstractAn efficient way to construct a library of isoxazoles and isoxazolines was developed by solution-phase 1,3-dipolar cycloaddition reaction of nitrile oxides with olefins and alkynes followed by precipitation of the products as HCl salts. (C) 2001 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleSolution-phase combinatorial synthesis of isoxazolines and isoxazoles using [2+3] cycloaddition reaction of nitrile oxides-
dc.typeArticle-
dc.identifier.doi10.1016/S0040-4039(00)02180-8-
dc.description.journalClass1-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.42, no.6, pp.1057 - 1060-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume42-
dc.citation.number6-
dc.citation.startPage1057-
dc.citation.endPage1060-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000166894400023-
dc.identifier.scopusid2-s2.0-0035808917-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordAuthorsolution-phas-
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