Intramolecular cyclization of C-2 symmetric and meso-iodo amino alcohols: A synthetic approach to azasugars

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dc.contributor.authorKang, SungHoko
dc.contributor.authorRyu, DHko
dc.date.accessioned2013-03-02T12:40:11Z-
dc.date.available2013-03-02T12:40:11Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1997-01-
dc.identifier.citationTETRAHEDRON LETTERS, v.38, no.4, pp.607 - 610-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10203/73560-
dc.description.abstractC-2 Symmetric and meso-iodo hydroxy ammonium chlorides generated from 2 and 5 have been cyclized under basic conditions to produce various heterocycles chemoselectively, which comprise tetrahydrofurans 7 and 19, piperidines 13, 15 and 21, and pyrrolidines 17 and 18. (C) 1997, Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectBIS-AZIRIDINES-
dc.subjectINHIBITION-
dc.subjectDERIVATIVES-
dc.subjectANALOGS-
dc.titleIntramolecular cyclization of C-2 symmetric and meso-iodo amino alcohols: A synthetic approach to azasugars-
dc.typeArticle-
dc.identifier.wosidA1997WD98800028-
dc.identifier.scopusid2-s2.0-0031023039-
dc.type.rimsART-
dc.citation.volume38-
dc.citation.issue4-
dc.citation.beginningpage607-
dc.citation.endingpage610-
dc.citation.publicationnameTETRAHEDRON LETTERS-
dc.contributor.localauthorKang, SungHo-
dc.contributor.nonIdAuthorRyu, DH-
dc.type.journalArticleArticle-
dc.subject.keywordPlusBIS-AZIRIDINES-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusANALOGS-
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