A stereoselective synthesis of 1-acetyl-2-aminomethylcyclopropanes from allylsulfonamides and phenyl(alkynyl)iodonium salts

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dc.contributor.authorLee, Hee Yoonko
dc.contributor.authorLee, YHko
dc.date.accessioned2013-03-04T18:04:59Z-
dc.date.available2013-03-04T18:04:59Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2001-10-
dc.identifier.citationSYNLETT, no.10, pp.1656 - 1658-
dc.identifier.issn0936-5214-
dc.identifier.urihttp://hdl.handle.net/10203/83554-
dc.description.abstractA versatile and stereoselective synthesis of 1-acetyl-2-aminomethyl cyclopropanes from the reaction of anions of tosylallylamines and phenyl(propynyl)iodonium salt was developed.-
dc.languageEnglish-
dc.publisherGEORG THIEME VERLAG KG-
dc.subjectINHIBITORS-
dc.titleA stereoselective synthesis of 1-acetyl-2-aminomethylcyclopropanes from allylsulfonamides and phenyl(alkynyl)iodonium salts-
dc.typeArticle-
dc.identifier.wosid000171453000052-
dc.type.rimsART-
dc.citation.issue10-
dc.citation.beginningpage1656-
dc.citation.endingpage1658-
dc.citation.publicationnameSYNLETT-
dc.contributor.localauthorLee, Hee Yoon-
dc.contributor.nonIdAuthorLee, YH-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorcarbenes-
dc.subject.keywordAuthorcycloadditions-
dc.subject.keywordAuthorhydrolysis-
dc.subject.keywordAuthorrearrangements-
dc.subject.keywordAuthorstereoselective synthesis-
dc.subject.keywordPlusINHIBITORS-
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