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Issue 44, 2018
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Controlled photorelease of alkynoic acids and their decarboxylative deprotection for copper-catalyzed azide/alkyne cycloaddition

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Abstract

A 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 reported.

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

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Publication details

The article was received on 24 Apr 2018, accepted on 03 May 2018 and first published on 15 May 2018


Article type: Communication
DOI: 10.1039/C8CC03341B
Citation: Chem. Commun., 2018,54, 5558-5561
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    Controlled photorelease of alkynoic acids and their decarboxylative deprotection for copper-catalyzed azide/alkyne cycloaddition

    N. Vohradská, E. M. Sánchez-Carnerero, T. Pastierik, C. Mazal and P. Klán, Chem. Commun., 2018, 54, 5558
    DOI: 10.1039/C8CC03341B

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