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Controlled photorelease of alkynoic acids and their decarboxylative deprotection for copper-catalyzed azide/alkyne cycloaddition

dc.contributor.authorVohradska, Nikoleta
dc.contributor.authorSanchez-Carnerero, E. M.
dc.contributor.authorPastierik, Tomas
dc.contributor.authorMazal, Ctibor
dc.contributor.authorKlán, Petr
dc.date.accessioned2024-01-22T15:14:20Z
dc.date.available2024-01-22T15:14:20Z
dc.date.issued2018-05-15
dc.identifier.citationChem. Commun., 2018,54, 5558-5561 BibTexes
dc.identifier.issn1359-7345
dc.identifier.urihttps://hdl.handle.net/10115/28656
dc.descriptionSupport for this work was provided by the Czech Science Foundation (GA13-25775S). The authors thank Marek Martı´nek for valuable help with technical issues, and Lucie Ludvı´kova´ for help in the determination of quantum yieldses
dc.description.abstractA controlled photorelease of alkynoic acids from the meso-methyl BODIPY photoremovable protecting group facilitates their subsequent efficient decarboxylation to give terminal alkynes for a CuI-catalyzed azide/alkyne cycloaddition. The quantum efficiencies of the photochemical step and the kinetics of the click reaction step are reportedes
dc.language.isoenges
dc.publisherRoyal Society of Chemistryes
dc.titleControlled photorelease of alkynoic acids and their decarboxylative deprotection for copper-catalyzed azide/alkyne cycloadditiones
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1039/c8cc03341bes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses


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