A STEREOCONTROLLED SYNTHESIS OF SYN-2,5-DISUBSTITUTED TETRAHYDROFURAN AND DIHYDROFURAN

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dc.contributor.authorKang, SungHoko
dc.contributor.authorLEE, SBko
dc.date.accessioned2013-02-24T10:54:44Z-
dc.date.available2013-02-24T10:54:44Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1993-11-
dc.identifier.citationTETRAHEDRON LETTERS, v.34, no.47, pp.7579 - 7582-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10203/56628-
dc.description.abstractIodoetherification of triethylsilyl ethers of trans-4-(3'-furanyl)-3-butenols has stereoselectively induced syn-2,5-disubstituted tetrahydrofurans 5s-10s, of which 5s has been readily converted into the corresponding dihydrofuran 21 and tetrahydrofuroate 22.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectTRANS-2,5-DISUBSTITUTED TETRAHYDROFURANS-
dc.subjectROUTE-
dc.subjectIODOETHERIFICATION-
dc.subjectINDUCTION-
dc.titleA STEREOCONTROLLED SYNTHESIS OF SYN-2,5-DISUBSTITUTED TETRAHYDROFURAN AND DIHYDROFURAN-
dc.typeArticle-
dc.identifier.wosidA1993MH25400021-
dc.identifier.scopusid2-s2.0-0027363043-
dc.type.rimsART-
dc.citation.volume34-
dc.citation.issue47-
dc.citation.beginningpage7579-
dc.citation.endingpage7582-
dc.citation.publicationnameTETRAHEDRON LETTERS-
dc.contributor.localauthorKang, SungHo-
dc.contributor.nonIdAuthorLEE, SB-
dc.type.journalArticleArticle-
dc.subject.keywordAuthor2,5-DIHYDROFURAN-
dc.subject.keywordAuthorFURANYL GROUP-
dc.subject.keywordAuthorIODOETHERIFICATION-
dc.subject.keywordAuthorSYN-2,5-DISUBSTITUTED TETRAHYDROFURANS-
dc.subject.keywordPlusTRANS-2,5-DISUBSTITUTED TETRAHYDROFURANS-
dc.subject.keywordPlusROUTE-
dc.subject.keywordPlusIODOETHERIFICATION-
dc.subject.keywordPlusINDUCTION-
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