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College of Natural Sciences(자연과학대학)Dept. of Chemistry(화학과)CH-Journal Papers(저널논문)

A facile deamination of aziridines using N2O4 under very mild conditions

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dc.contributor.authorLee, Kko
dc.contributor.authorKim, Yong Haeko
dc.date.accessioned2013-02-27T09:15:49Z-
dc.date.available2013-02-27T09:15:49Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1999-
dc.identifier.citationSYNTHETIC COMMUNICATIONS, v.29, no.7, pp.1241 - 1248-
dc.identifier.issn0039-7911-
dc.identifier.urihttp://hdl.handle.net/10203/67697-
dc.description.abstractVarious aziridines reacted with N2O4 (2 eq) in the presence of Et3N ( 1 or 2 eq) in dry THF to give the corresponding ethylenes in good to excellent yields at (-23 degrees C or -43 degrees C) in 10 min under Ar.-
dc.languageEnglish-
dc.publisherMARCEL DEKKER INC-
dc.subjectDINITROGEN TETROXIDE-
dc.subjectPYRROLIZIDINE ALKALOIDS-
dc.subjectCONVERSION-
dc.subjectDERIVATIVES-
dc.subjectEXPANSION-
dc.subjectAZIDES-
dc.subjectACIDS-
dc.titleA facile deamination of aziridines using N2O4 under very mild conditions-
dc.typeArticle-
dc.identifier.wosid000079162800022-
dc.type.rimsART-
dc.citation.volume29-
dc.citation.issue7-
dc.citation.beginningpage1241-
dc.citation.endingpage1248-
dc.citation.publicationnameSYNTHETIC COMMUNICATIONS-
dc.identifier.doi10.1080/00397919908086096-
dc.contributor.nonIdAuthorLee, K-
dc.type.journalArticleArticle-
dc.subject.keywordPlusDINITROGEN TETROXIDE-
dc.subject.keywordPlusPYRROLIZIDINE ALKALOIDS-
dc.subject.keywordPlusCONVERSION-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusEXPANSION-
dc.subject.keywordPlusAZIDES-
dc.subject.keywordPlusACIDS-
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