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Synthesis and antifungal activities of furoxan derivatives designed as novel fungicide

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dc.contributor.authorHwang, K.-J.-
dc.contributor.authorPark, Y.C.-
dc.contributor.authorKim, H.J.-
dc.contributor.authorLee, J.H.-
dc.date.accessioned2022-05-19T02:40:43Z-
dc.date.available2022-05-19T02:40:43Z-
dc.date.created2022-05-19-
dc.date.issued1998-
dc.identifier.issn0916-8451-
dc.identifier.urihttps://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/27757-
dc.description.abstractFuroxan derivatives 3-11 were designed and synthesized as potential fungicides. Symmetrically substituted furoxan derivatives 3a-j were prepared by dimerization of the corresponding nitrile oxide generated from N-hydroxyliminoyl chloride 2 in situ. Further functional group modifications of aldehyde 4, a key intermediate, generated furoxan derivatives 5-11. The fungicidal activities of furoxan derivatives 3-11 were observed over a broad spectrum of plant fungi at 250 ppm. © 1998, Taylor & Francis Group, LLC. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.titleSynthesis and antifungal activities of furoxan derivatives designed as novel fungicide-
dc.typeArticle-
dc.contributor.affiliatedAuthorHwang, K.-J.-
dc.identifier.doi10.1271/bbb.62.1693-
dc.identifier.scopusid2-s2.0-0001548894-
dc.identifier.bibliographicCitationBioscience, Biotechnology and Biochemistry, v.62, no.9, pp.1693 - 1697-
dc.relation.isPartOfBioscience, Biotechnology and Biochemistry-
dc.citation.titleBioscience, Biotechnology and Biochemistry-
dc.citation.volume62-
dc.citation.number9-
dc.citation.startPage1693-
dc.citation.endPage1697-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordAuthorFungicidal activity-
dc.subject.keywordAuthorFurazan N-oxide-
dc.subject.keywordAuthorFuroxan-
dc.subject.keywordAuthorWheat leaf rust-
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