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dc.contributor.authorZhan, Zhuang-ping
dc.contributor.author詹庒平
dc.contributor.authorYu, Jing-liang
dc.contributor.authorLiu, Hui-juan
dc.contributor.authorCui, Yuan-yuan
dc.contributor.authorYang, Rui-feng
dc.contributor.authorYang, Wen-zhen
dc.contributor.authorLi, Jun-ping
dc.date.accessioned2011-07-03T02:16:48Z
dc.date.available2011-07-03T02:16:48Z
dc.date.issued2006-09
dc.identifier.citationJ. Org. Chem., 2006, 71 (21): 8298–8301zh_CN
dc.identifier.issn0022-3263
dc.identifier.urihttp://dx.doi.org/doi:10.1021/jo061234p
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/9944
dc.description.abstractA general and efficient FeCl3-catalyzed substitution reaction of propargylic alcohols with carbon- and heteroatom-centered nucleophiles such as allyl trimethylsilane, alcohols, aromatic compounds, thiols, and amides, leading to the construction of C-C, C-O, C-S and C-N bonds, has been developed.zh_CN
dc.language.isoenzh_CN
dc.publisherAMER CHEMICAL SOCzh_CN
dc.titleA general and efficient FeCl3-catalyzed nucleophilic substitution of propargylic alcoholszh_CN
dc.typeArticlezh_CN


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