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dc.contributor.authorChen, Hong-Bin
dc.contributor.authorZhao, Yan
dc.contributor.authorLiao, Yi
dc.date.accessioned2015-09-21T20:16:48Z
dc.date.available2015-09-21T20:16:48Z
dc.date.issued2015-04-13
dc.identifier.citationChen, H. B., Zhao, Y., & Liao, Y. (2015). Aldehyde–alkyne–amine (A 3) coupling catalyzed by a highly efficient dicopper complex. RSC Advances, 5(47), 37737-37741.en_US
dc.identifier.urihttp://hdl.handle.net/11141/750
dc.description.abstractA dicopper(I) complex, CuI 2ðpipÞ 2 (pip ¼ (2-picolyliminomethyl)pyrrole anion), was utilized to catalyze A3 coupling reactions, which led to the formation of propargylamines. Aldehydes, alkynes and amines with a variety of structures have been tested. A low catalyst loading of 0.4 mol% was sufficient to give good to excellent yields. The low catalyst loading, broad scope of substrate and easy preparation make this dicopper complex a useful catalyst for A3 coupling.en_US
dc.language.isoen_USen_US
dc.rightsThis published article is available in accordance with the publisher's policy. It may be subject to U.S. copyright law.en_US
dc.rights.urihttp://www.rsc.org/journals-books-databases/journal-authors-reviewers/licences-copyright-permissions/en_US
dc.titleAldehyde–alkyne–amine (A3) coupling catalyzed by a highly efficient dicopper complexen_US
dc.typePostprinten_US
dc.identifier.doi10.1039/c5ra04729c


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