Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/100845
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dc.contributor.authorChung-Yen Lizh_TW
dc.contributor.authorChin-Fa Leezh_TW
dc.contributor.authorDaggula Mallikarjuna Reddyzh_TW
dc.contributor.authorYi-Xuan Lizh_TW
dc.contributor.authorYou-Chen Liuzh_TW
dc.date.accessioned2023-03-30T06:38:20Z-
dc.date.available2023-03-30T06:38:20Z-
dc.identifier.urihttp://hdl.handle.net/11455/100845-
dc.description.abstractWe report herein a new approach for the synthesis of organothiophosphates from phosphonates and thiols through electrochemical reaction. The reactions were conducted without the addition of oxidant, transition-metal base, or base at room temperature. This system has a good substrate scope and functional group tolerance. Aryl and alkyl thiols worked well with phosphonates to afford the corresponding organothiophosphates in good yields.zh_TW
dc.language.isoenzh_TW
dc.titleElectrochemical Dehydrogenative Phosphorylation of Thiolszh_TW
dc.typejournal articlezh_TW
item.openairetypejournal article-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.fulltextwith fulltext-
item.grantfulltextopen-
item.languageiso639-1en-
item.cerifentitytypePublications-
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