Reaction of Pummerer Rearrangement Intermediate with Thiols: New Synthetic Method of S,S-Thioacetals of Formylphosphonate

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dc.contributor.authorOh, Dong Youngko
dc.date.accessioned2013-02-25T21:29:10Z-
dc.date.available2013-02-25T21:29:10Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued1994-
dc.identifier.citationSYNTHETIC COMMUNICATIONS, v.24, no.16, pp.2313 - 2318-
dc.identifier.issn0039-7911-
dc.identifier.urihttp://hdl.handle.net/10203/65442-
dc.description.abstractPummerer rearrangement reaction intermediate 2) of phenylsulfinyl methanephosphonate(1) has been found to react mildly with thiols(3) in the presence of stannic chloride to provide S,S-thioacetals of formylphosphonate(4).-
dc.languageEnglish-
dc.publisherTaylor & Francis Inc-
dc.subjectCARBANIONS-
dc.titleReaction of Pummerer Rearrangement Intermediate with Thiols: New Synthetic Method of S,S-Thioacetals of Formylphosphonate-
dc.typeArticle-
dc.identifier.wosidA1994NY15900011-
dc.type.rimsART-
dc.citation.volume24-
dc.citation.issue16-
dc.citation.beginningpage2313-
dc.citation.endingpage2318-
dc.citation.publicationnameSYNTHETIC COMMUNICATIONS-
dc.type.journalArticleArticle-
dc.subject.keywordPlusCARBANIONS-
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