New cyclization of N-hydroxyiminoyl chlorides with N-alkryl ethynesulfonamides: Synthesis of 4-alkyl-3-aryl-4,5-dihydro-1,5,2,4-oxathiadiazepine-5,5-diones

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dc.contributor.authorLee, YSko
dc.contributor.authorChung, KHko
dc.contributor.authorKim, Yong Haeko
dc.date.accessioned2013-02-27T10:18:28Z-
dc.date.available2013-02-27T10:18:28Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1999-
dc.identifier.citationHETEROATOM CHEMISTRY, v.10, no.6, pp.461 - 464-
dc.identifier.issn1042-7163-
dc.identifier.urihttp://hdl.handle.net/10203/67940-
dc.description.abstractN-Hydroxyiminoyl chlorides reacted With N-alkyl ethynesulfonamides in the presence of triethylamine in CH,CZ, to afford the 4-alkyl-3-aryl-4,5dihydro-1,5,2,4-oxathiadiazepine-5, 5-diones (3) as the major products together with N-alkyl-3-aryl-5-isoxazolesulfonamides (4). (C) 1999 John Wiley & Sons, Inc.-
dc.languageEnglish-
dc.publisherJOHN WILEY SONS INC-
dc.subjectNITRILE OXIDES-
dc.subjectCYCLO-ADDITIONS-
dc.subject1,3-DIPOLAR CYCLOADDITIONS-
dc.subjectREGIOCHEMISTRY-
dc.subjectSELECTIVITY-
dc.titleNew cyclization of N-hydroxyiminoyl chlorides with N-alkryl ethynesulfonamides: Synthesis of 4-alkyl-3-aryl-4,5-dihydro-1,5,2,4-oxathiadiazepine-5,5-diones-
dc.typeArticle-
dc.identifier.wosid000082588000004-
dc.type.rimsART-
dc.citation.volume10-
dc.citation.issue6-
dc.citation.beginningpage461-
dc.citation.endingpage464-
dc.citation.publicationnameHETEROATOM CHEMISTRY-
dc.identifier.doi10.1002/(SICI)1098-1071(1999)10:6<461::AID-HC4>3.0.CO;2-7-
dc.contributor.nonIdAuthorLee, YS-
dc.contributor.nonIdAuthorChung, KH-
dc.type.journalArticleArticle-
dc.subject.keywordPlusNITRILE OXIDES-
dc.subject.keywordPlusCYCLO-ADDITIONS-
dc.subject.keywordPlus1,3-DIPOLAR CYCLOADDITIONS-
dc.subject.keywordPlusREGIOCHEMISTRY-
dc.subject.keywordPlusSELECTIVITY-
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