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dc.contributor.authorHao, Lu
dc.contributor.authorWu, Feng
dc.contributor.authorDing, Zong-Cang
dc.contributor.authorXu, Su-Xia
dc.contributor.authorMa, Yan-Li
dc.contributor.authorChen, Li
dc.contributor.authorZhan, Zhuang-Ping
dc.contributor.author詹庄平
dc.date.accessioned2013-04-07T01:53:15Z
dc.date.available2013-04-07T01:53:15Z
dc.date.issued2012-05
dc.identifier.citationCHEMISTRY-A EUROPEAN JOURNAL,2012,18(21):6453-6456zh_CN
dc.identifier.issn0947-6539
dc.identifier.urihttp://dx.doi.org/10.1002/chem.201200763
dc.identifier.uriWOS:000304045000008
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/15509
dc.description.abstractNontoxic cyanide source: An unprecedented route to acrylonitriles by employing propargylic alcohols and para-tolylsulfonohydrazide as a combined cyano source has been developed (see scheme). This efficient and practical cyanation reaction proceeds through an FeCl3-catalyzed domino propargylic substitution/aza-Meyer–Schuster rearrangement sequence, the rearrangement process of which is reported for the first time.zh_CN
dc.description.sponsorshipNSFC [21072159]; 973 Projects [2011CB935901]; NFFTBS [J1030415]; Science & Technology Bureau of Xiamen [3502Z20093007]zh_CN
dc.language.isoenzh_CN
dc.publisherWILEY-V C H VERLAG GMBHzh_CN
dc.subjectacrylonitrileszh_CN
dc.subjectcyanideszh_CN
dc.subjectdomino reactionszh_CN
dc.subjectironzh_CN
dc.subjectpropargylic substitutionzh_CN
dc.subjectrearrangementzh_CN
dc.titleSynthesis of Acrylonitriles through an FeCl3-Catalyzed Domino Propargylic Substitution/Aza-Meyer-Schuster Rearrangement Sequencezh_CN
dc.typeArticlezh_CN


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