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A modified procedure for the synthesis of 5-amino-3-arylisoxazoles and their reactions with tetrasulfur tetranitride antimony(V) chloride complex (S4N4 center dot SbCl5): Novel synthesis of 3-aryl-1,2,5-thiadiazole-4-carboxamides

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dc.contributor.authorKong, YC-
dc.contributor.authorKim, K-
dc.contributor.authorPark, YJ-
dc.date.available2021-02-22T16:46:16Z-
dc.date.created2020-09-01-
dc.date.issued2001-01-01-
dc.identifier.issn0385-5414-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/16683-
dc.description.abstractDropwise addition of alpha -bromo ketoximes to a solution of KCN in MeOH at room temperature gave 5-amino-3-arylisoxazoles in moderate to good yields. Treatment of the isoxazoles prepared with tetrasulfur tetranitride antimony (V) chloride complex (S4N4. SbCl5) in toluene at 100 degreesC afforded novel 3-aryl-1,2,5-thiadiazole-4-carboxamides.-
dc.language영어-
dc.language.isoen-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleA modified procedure for the synthesis of 5-amino-3-arylisoxazoles and their reactions with tetrasulfur tetranitride antimony(V) chloride complex (S4N4 center dot SbCl5): Novel synthesis of 3-aryl-1,2,5-thiadiazole-4-carboxamides-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, YJ-
dc.identifier.wosid000167581900011-
dc.identifier.bibliographicCitationHETEROCYCLES, v.55, no.1, pp.75 - 89-
dc.relation.isPartOfHETEROCYCLES-
dc.citation.titleHETEROCYCLES-
dc.citation.volume55-
dc.citation.number1-
dc.citation.startPage75-
dc.citation.endPage89-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
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