Benjamin Boëns
University of Limoges
14 Papers
126 Citations
Benjamin Boëns is an academic researcher from University of Limoges. The author has contributed to research in topics: Click chemistry & Catalysis. The author has an hindex of 5, co-authored 14 publications. Previous affiliations of Benjamin Boëns include Lucideon.
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Papers
Polysaccharides: The “Click” Chemistry Impact
Pierre-Henri Elchinger,Pierre-Antoine Faugeras,Benjamin Boëns,François Brouillette,Daniel Montplaisir,Rachida Zerrouki,Romain Lucas +6 more
TL;DR: The present review summarizes the contribution of "click" chemistry in the world of polysaccharides and particularly the copper-catalyzed version of the Huisgen 1,3-dipolar cycloaddition reaction between terminal acetylenes and azides.
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When Cyclodextrins Meet Click Chemistry
Pierre-Antoine Faugeras,Benjamin Boëns,Pierre-Henri Elchinger,François Brouillette,Daniel Montplaisir,Rachida Zerrouki,Romain Lucas +6 more
TL;DR: In this paper, the role of click chemistry in cyclic oligosaccharides is discussed, focusing on the different areas of chemistry, including chromatography, biological applications, the elaboration of superstructures, and metal detection.
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Iodine-catalyzed one-pot synthesis of unsymmetrical meso-substituted porphyrins
Benjamin Boëns,Pierre-Antoine Faugeras,Julien Vergnaud,Romain Lucas,Karine Teste,Rachida Zerrouki +5 more
TL;DR: In this paper, an iodine-catalyzed one-pot synthesis of 5-(4-nitrophenyl)-10,15,20-triphenylporphyrin is described.
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Synthesis of meso-substituted dipyrromethanes using iodine-catalysis
Pierre-Antoine Faugeras,Benjamin Boëns,Pierre-Henri Elchinger,Julien Vergnaud,Karine Teste,Rachida Zerrouki +5 more
TL;DR: In this paper, a non-conventional synthesis of meso-substituted dipyrromethanes, using molecular iodine as the catalyst, was presented, which was obtained in good yields after a preliminary study using nitrobenzaldehyde.
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New thymine-based derivative of nitrogen mustards.
TL;DR: This work deals with the synthesis of a new nitrogen mustard derivative based on thymine thanks to a synthetic pathway in five steps that introduces the bis(2-chloroethyl)amine group to position 4 of the pyrimidine base.
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