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dc.contributor.authorZhan, Zhuang-Ping
dc.contributor.author詹庄平
dc.contributor.authorWang, Shao-Pei
dc.contributor.authorCai, Xu-Bin
dc.contributor.authorLiu, Hui-Juan
dc.contributor.authorYu, Jing-Liang
dc.contributor.authorCui, Yuan-Yuan
dc.date.accessioned2011-05-30T15:39:52Z
dc.date.available2011-05-30T15:39:52Z
dc.date.issued2007-09
dc.identifier.citationADVANCED SYNTHESIS & CATALYSIS,2007,349(130:2097-2102zh_CN
dc.identifier.issn1615-4150
dc.identifier.urihttp://dx.doi.org/doi:10.1002/adsc.200700234
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/9293
dc.description.abstractA novel and efficient procedure for the synthesis of gamma-alkynyl ketones by the nucleophilic substitution of propargylic acetates with enoxysilanes in the presence of a catalytic amount of Copper(II) triflate, has been developed. The substitution reaction can be followed by a 4-toluenesulfonic acid-catalyzed cyclization without purification of the gamma-alkynyl ketone intermediates, offering a straightforward synthetic route to polysubstituted furans.zh_CN
dc.language.isoenzh_CN
dc.publisherWILEY-V C H VERLAG GMBHzh_CN
dc.subjectcopper(II) triflatezh_CN
dc.subjectenoxysilaneszh_CN
dc.subjectfuranszh_CN
dc.subjectnucleophilic substitutionzh_CN
dc.subjectpropargylic acetateszh_CN
dc.titleCopper(H) triflate-catalyzed nucleophilic substitution of propargylic acetates with enoxysilanes. A straightforward synthetic route to polysubstituted furanszh_CN
dc.typeArticlezh_CN


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