Show simple item record

dc.contributor.authorZhan, Zhuang-ping
dc.contributor.author詹庄平
dc.contributor.authorYang, Wen-zhen
dc.contributor.authorYang, Rui-feng
dc.contributor.authorYu, Jing-liang
dc.contributor.authorLi, Jun-ping
dc.contributor.authorLiu, Hui-juan
dc.date.accessioned2011-08-01T13:06:43Z
dc.date.available2011-08-01T13:06:43Z
dc.date.issued2006-06
dc.identifier.citationCHEMICAL COMMUNICATIONS,2006,31:3352-3354zh_CN
dc.identifier.issn1359-7345
dc.identifier.urihttp://dx.doi.org/doi:10.1039/B606470A
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/10353
dc.description.abstractA general and efficient BiCl3-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.publisherROYAL SOC CHEMISTRYzh_CN
dc.titleBiCl3-catalyzed propargylic substitution reaction of propargylic alcohols with C-, O-, S- and N-centered nucleophileszh_CN
dc.typeArticlezh_CN


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record