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dc.contributor.authorZhan, Zhuang-Ping
dc.contributor.author詹庄平
dc.contributor.authorCai, Xu-Bin
dc.contributor.authorWang, Shao-Pei
dc.contributor.authorYu, Jing-Liang
dc.contributor.authorLiu, Hui-Juan
dc.contributor.authorCui, Yuan-Yuan
dc.date.accessioned2011-05-28T02:22:18Z
dc.date.available2011-05-28T02:22:18Z
dc.date.issued2007-11
dc.identifier.citationJ. Org. Chem., 2007, 72 (25):9838–9841zh_CN
dc.identifier.issn0022-3263
dc.identifier.urihttp://dx.doi.org/doi:10.1021/jo701782g
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/9220
dc.description.abstract[Graphics] An efficient FeCl3-catalyzed substitution reaction of propargylic acetates with enoxysilanes under mild conditions to afford corresponding gamma-alkynyl ketones has been developed. The substitution reaction is followed by a TsOH-catalyzed cyclization without purification of the gamma-alkynyl ketone intermediates, offering a straightforward synthetic route to tri- or tetrasubstituted furans.zh_CN
dc.language.isoenzh_CN
dc.publisherAMER CHEMICAL SOCzh_CN
dc.titleFeCl3-catalyzed nucleophilic substitution of propargylic acetates with enoxysilaneszh_CN
dc.typeArticlezh_CN


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