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dc.contributor.authorWeng, Zhiqiang
dc.contributor.authorLi, Huaifeng
dc.contributor.authorHe, Weiming
dc.contributor.authorYao, Liangfeng
dc.contributor.authorTan, Jianwei
dc.contributor.authorChen, Jinfa
dc.contributor.authorYuan, Yaofeng
dc.contributor.authorHuang, Kuo-Wei
dc.date.accessioned2015-08-03T09:45:16Z
dc.date.available2015-08-03T09:45:16Z
dc.date.issued2012-03
dc.identifier.issn00404020
dc.identifier.doi10.1016/j.tet.2011.12.085
dc.identifier.urihttp://hdl.handle.net/10754/562120
dc.description.abstractA catalytic process for trifluoromethylation of terminal alkynes with Togni's reagent has been developed, affording trifluoromethylated acetylenes in good to excellent yields. The reaction is conducted at room temperature and exhibits tolerance to a range of functional groups. © 2012 Elsevier Ltd. All rights reserved.
dc.description.sponsorshipWe acknowledge the financial support from King Abdullah University of Science and Technology to K.-W.H. and from National Natural Science Foundation of China (21072030) and Fuzhou University (022318) to Z.W.
dc.publisherElsevier BV
dc.subjectCopper catalyst
dc.subjectTerminal alkyne
dc.subjectTrifluoromethylation reaction
dc.titleMild copper-catalyzed trifluoromethylation of terminal alkynes using an electrophilic trifluoromethylating reagent
dc.typeArticle
dc.contributor.departmentBiological and Environmental Sciences and Engineering (BESE) Division
dc.contributor.departmentChemical Science Program
dc.contributor.departmentHomogeneous Catalysis Laboratory (HCL)
dc.contributor.departmentKAUST Catalysis Center (KCC)
dc.contributor.departmentPhysical Science and Engineering (PSE) Division
dc.identifier.journalTetrahedron
dc.contributor.institutionDepartment of Chemistry, Fuzhou University, Fujian 350108, China
kaust.personLi, Huaifeng
kaust.personYao, Liangfeng
kaust.personHuang, Kuo-Wei


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