DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lee, YS | ko |
dc.contributor.author | Chung, KH | ko |
dc.contributor.author | Kim, Yong Hae | ko |
dc.date.accessioned | 2013-02-27T10:18:28Z | - |
dc.date.available | 2013-02-27T10:18:28Z | - |
dc.date.created | 2012-02-06 | - |
dc.date.created | 2012-02-06 | - |
dc.date.issued | 1999 | - |
dc.identifier.citation | HETEROATOM CHEMISTRY, v.10, no.6, pp.461 - 464 | - |
dc.identifier.issn | 1042-7163 | - |
dc.identifier.uri | http://hdl.handle.net/10203/67940 | - |
dc.description.abstract | N-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.language | English | - |
dc.publisher | JOHN WILEY SONS INC | - |
dc.subject | NITRILE OXIDES | - |
dc.subject | CYCLO-ADDITIONS | - |
dc.subject | 1,3-DIPOLAR CYCLOADDITIONS | - |
dc.subject | REGIOCHEMISTRY | - |
dc.subject | SELECTIVITY | - |
dc.title | 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 | - |
dc.type | Article | - |
dc.identifier.wosid | 000082588000004 | - |
dc.type.rims | ART | - |
dc.citation.volume | 10 | - |
dc.citation.issue | 6 | - |
dc.citation.beginningpage | 461 | - |
dc.citation.endingpage | 464 | - |
dc.citation.publicationname | HETEROATOM CHEMISTRY | - |
dc.identifier.doi | 10.1002/(SICI)1098-1071(1999)10:6<461::AID-HC4>3.0.CO;2-7 | - |
dc.contributor.nonIdAuthor | Lee, YS | - |
dc.contributor.nonIdAuthor | Chung, KH | - |
dc.type.journalArticle | Article | - |
dc.subject.keywordPlus | NITRILE OXIDES | - |
dc.subject.keywordPlus | CYCLO-ADDITIONS | - |
dc.subject.keywordPlus | 1,3-DIPOLAR CYCLOADDITIONS | - |
dc.subject.keywordPlus | REGIOCHEMISTRY | - |
dc.subject.keywordPlus | SELECTIVITY | - |
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