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dc.contributor.authorWang, Tao
dc.contributor.authorChen, Xin-liang
dc.contributor.authorChen, Li
dc.contributor.authorZhan, Zhuang-ping
dc.contributor.author詹庄平
dc.date.accessioned2012-03-04T09:35:05Z
dc.date.available2012-03-04T09:35:05Z
dc.date.issued2011-06-07
dc.identifier.citationORGANIC LETTERS,2011,13(13):3324-3327zh_CN
dc.identifier.issn1523-7060
dc.identifier.urihttp://dx.doi.org/doi:10.1021/ol201054z
dc.identifier.uriWOS:000291920800010
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/11605
dc.description.abstractUnder different conditions, the reaction of propargyl alcohols and terminal alkynes leads to the selective formation of 1,4-diynes and polysubstituted furans/pyrroles. Water is the only byproduct in the selective synthesis of 1,4-diynes and pyrroles, and the strategy for the furan synthesis is of 100% atom economy.zh_CN
dc.description.sponsorshipNational Nature Science Foundation of China[21072159]zh_CN
dc.language.isoenzh_CN
dc.publisherAMER CHEMICAL SOCzh_CN
dc.titleAtom-Economical Chemoselective Synthesis of 1,4-Diynes and Polysubstituted Furans/Pyrroles from Propargyl Alcohols and Terminal Alkyneszh_CN
dc.typeArticlezh_CN


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