Stereoselective Halolactonization of $\alpha$-Phenylsulfonyl-$\gamma, \delta$-unsaturated Amides

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dc.contributor.authorJ.W. Leeko
dc.contributor.authorJ.W. Jungko
dc.contributor.authorOh, Dong Youngko
dc.date.accessioned2013-02-25T16:18:52Z-
dc.date.available2013-02-25T16:18:52Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1994-
dc.identifier.citationBULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.15, no.10, pp.842 - 845-
dc.identifier.issn0253-2964-
dc.identifier.urihttp://hdl.handle.net/10203/63488-
dc.description.abstractIodine-induced lactonization of alpha-phenylsulfonyl-gamma,delta-unsaturated amides provided 2-4-trans-substitued gamma-butyrolactones in high selectivity. NBS-or NCS-induced lactonization of N,N-dimethyl-2-(phenylsulfonyl)-4-pentenamide in DME-H2O(2:1 vol) gave 2-halo-4-(halomethyl)-2-(phenylsulfonyl)-gamma-butyrolactone.-
dc.languageEnglish-
dc.publisherKorean Chemical Soc-
dc.subjectBETA-KETO SULFONES-
dc.titleStereoselective Halolactonization of $\alpha$-Phenylsulfonyl-$\gamma, \delta$-unsaturated Amides-
dc.typeArticle-
dc.identifier.wosidA1994PR03000012-
dc.type.rimsART-
dc.citation.volume15-
dc.citation.issue10-
dc.citation.beginningpage842-
dc.citation.endingpage845-
dc.citation.publicationnameBULLETIN OF THE KOREAN CHEMICAL SOCIETY-
dc.contributor.nonIdAuthorJ.W. Lee-
dc.contributor.nonIdAuthorJ.W. Jung-
dc.type.journalArticleArticle-
dc.subject.keywordPlusBETA-KETO SULFONES-
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