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Highly diastereoselective synthesis of substituted cyclopentenes through multicomponent reactions of phosphines, enynedioates, and benzylidene malononitriles via an unexpected phosphine alpha-addition-delta-evolvement of an anion pathway

dc.citation.volume251en_US
dc.contributor.authorChuang, Shih-Chingen_US
dc.contributor.authorSung, Shih-Pingen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2018-08-21T05:53:39Z
dc.date.available2018-08-21T05:53:39Z
dc.date.issued2016-03-13en_US
dc.identifier.issn0065-7727en_US
dc.identifier.journalABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETYen_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/144970
dc.identifier.wosnumberWOS:000431905704304en_US
dc.language.isoen_USen_US
dc.titleHighly diastereoselective synthesis of substituted cyclopentenes through multicomponent reactions of phosphines, enynedioates, and benzylidene malononitriles via an unexpected phosphine alpha-addition-delta-evolvement of an anion pathwayen_US
dc.typeArticleen_US

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