SYNTHETIC ROUTE TO ALPHA -PHOSPHONO-GAMMA -BUTYROLACTONES : SYNTHESIS OF GAMMA -SUBSTITUTED ALPHA -METHYLENE-GAMMA -BUTYRO-LACTONES

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dc.contributor.authorC. W. Leeko
dc.contributor.authorJ. M. Gilko
dc.contributor.authorOh, Dong Youngko
dc.date.accessioned2013-02-28T04:17:44Z-
dc.date.available2013-02-28T04:17:44Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1997-
dc.identifier.citationHETEROCYCLES, v.45, no.5, pp.943 - 948-
dc.identifier.issn0385-5414-
dc.identifier.urihttp://hdl.handle.net/10203/72736-
dc.description.abstractTreatment of lithiated homoallylic phosphonates with dimethyl carbamyl chloride gave 2-amidophosphonate derivatives. A solution of 2-amidophosphonate in DME-H2O (2:1 vol) reacted with 2 eq. iodine at room temperature to give alpha-phosphono-gamma-iodoalkyl-gamma-butyrolactones in good yield, although the products are mixture. Wadsworth-Emmons reaction of alpha-phosphono-gamma-iodoalkyl-gamma-butyrolactones with aldehydes gave alpha-(alkyl)methylene-gamma-iodoalkyl-gamma-butyro-lactone derivatives.-
dc.languageEnglish-
dc.publisherPergamon-Elsevier Science Ltd-
dc.subjectSTEREOSELECTIVE SYNTHESIS-
dc.subjectEFFICIENT SYNTHESIS-
dc.subjectDERIVATIVES-
dc.subjectCARBANION-
dc.subjectLACTONES-
dc.titleSYNTHETIC ROUTE TO ALPHA -PHOSPHONO-GAMMA -BUTYROLACTONES : SYNTHESIS OF GAMMA -SUBSTITUTED ALPHA -METHYLENE-GAMMA -BUTYRO-LACTONES-
dc.typeArticle-
dc.identifier.wosidA1997XG65500014-
dc.identifier.scopusid2-s2.0-0000212979-
dc.type.rimsART-
dc.citation.volume45-
dc.citation.issue5-
dc.citation.beginningpage943-
dc.citation.endingpage948-
dc.citation.publicationnameHETEROCYCLES-
dc.contributor.nonIdAuthorC. W. Lee-
dc.contributor.nonIdAuthorJ. M. Gil-
dc.type.journalArticleArticle-
dc.subject.keywordPlusSTEREOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusEFFICIENT SYNTHESIS-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusCARBANION-
dc.subject.keywordPlusLACTONES-
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