A STEREOCONTROLLED SYNTHESIS OF ANTI-2,5-DISUBSTITUTED TETRAHYDROFURANS

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dc.contributor.authorKang, SungHoko
dc.contributor.authorLEE, SBko
dc.date.accessioned2013-02-25T21:30:59Z-
dc.date.available2013-02-25T21:30:59Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1993-03-
dc.identifier.citationTETRAHEDRON LETTERS, v.34, no.12, pp.1955 - 1958-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10203/65453-
dc.description.abstractAnti-2,5-disubstituted tetrahydrofurans, in which one of the substituents is 3'-furanyl group, have been derived from trans-4-(3'-furanyl)-3-butenols 3-8 by using iodine in diethyl ether in the presence of potassium carbonate at -78-degrees-C.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectTRANS-2,5-DISUBSTITUTED TETRAHYDROFURANS-
dc.subjectABSOLUTE-CONFIGURATION-
dc.subjectIODOETHERIFICATION-
dc.subjectVERRUCOSIDIN-
dc.subjectINDUCTION-
dc.subjectROUTE-
dc.titleA STEREOCONTROLLED SYNTHESIS OF ANTI-2,5-DISUBSTITUTED TETRAHYDROFURANS-
dc.typeArticle-
dc.identifier.wosidA1993KU30600029-
dc.identifier.scopusid2-s2.0-0027467073-
dc.type.rimsART-
dc.citation.volume34-
dc.citation.issue12-
dc.citation.beginningpage1955-
dc.citation.endingpage1958-
dc.citation.publicationnameTETRAHEDRON LETTERS-
dc.contributor.localauthorKang, SungHo-
dc.contributor.nonIdAuthorLEE, SB-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorDIHYDROFURANS-
dc.subject.keywordAuthorFURANYL GROUP-
dc.subject.keywordAuthorIODOETHERIFICATION-
dc.subject.keywordAuthorANTI-2,5-DISUBSTITUTED TETRAHYDROFURANS-
dc.subject.keywordPlusTRANS-2,5-DISUBSTITUTED TETRAHYDROFURANS-
dc.subject.keywordPlusABSOLUTE-CONFIGURATION-
dc.subject.keywordPlusIODOETHERIFICATION-
dc.subject.keywordPlusVERRUCOSIDIN-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordPlusROUTE-
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CH-Journal Papers(저널논문)
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