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.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.identifier.citationChem. Commun., 2018,54, 5558-5561 BibTexes
dc.identifier.doi10.1039/c8cc03341bes
dc.identifier.issn1359-7345
dc.identifier.urihttps://hdl.handle.net/10115/28656
dc.language.isoenges
dc.publisherRoyal Society of Chemistryes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.titleControlled photorelease of alkynoic acids and their decarboxylative deprotection for copper-catalyzed azide/alkyne cycloadditiones
dc.typeinfo:eu-repo/semantics/articlees

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Chemical Communications, 2018, 54(44), pp. 5558–5561.pdf
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