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dc.contributor.authorDherbassy, Quentin
dc.contributor.authorManna, Srimanta; orcid: 0000-0002-3903-1256
dc.contributor.authorTalbot, Fabien J T
dc.contributor.authorPrasitwatcharakorn, Watcharapon
dc.contributor.authorPerry, Gregory J P; orcid: 0000-0001-8173-3369
dc.contributor.authorProcter, David J; orcid: 0000-0003-3179-2509
dc.date.accessioned2021-07-09T01:08:09Z
dc.date.available2021-07-09T01:08:09Z
dc.date.issued2020-10-07
dc.identifierhttps://chesterrep.openrepository.com/bitstream/handle/10034/625198/article.pdf?sequence=2
dc.identifier.citationChemical science, volume 11, issue 42, page 11380-11393
dc.identifier.urihttp://hdl.handle.net/10034/625198
dc.descriptionFrom Europe PMC via Jisc Publications Router
dc.descriptionHistory: ppub 2020-10-01, epub 2020-10-07
dc.descriptionPublication status: Published
dc.descriptionFunder: Engineering and Physical Sciences Research Council; Grant(s): EP/P001386/1, EP/M005062/1
dc.description.abstractThe copper-catalyzed functionalization of enyne derivatives has recently emerged as a powerful approach in contemporary synthesis. Enynes are versatile and readily accessible substrates that can undergo a variety of reactions to yield densely functionalized, enantioenriched products. In this perspective, we review copper-catalyzed transformations of enynes, such as boro- and hydrofunctionalizations, copper-mediated radical difunctionalizations, and cyclizations. Particular attention is given to the regiodivergent functionalization of 1,3-enynes, and the current mechanistic understanding of such processes.
dc.languageeng
dc.rightsLicence for this article: cc by
dc.sourceissn: 2041-6520
dc.sourceessn: 2041-6539
dc.sourcenlmid: 101545951
dc.titleCopper-catalyzed functionalization of enynes.
dc.typearticle
dc.date.updated2021-07-09T01:08:09Z


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