Davide Arnodo
University of Turin
12 Papers
1 Citations
Davide Arnodo is an academic researcher from University of Turin. The author has contributed to research in topics: Chemistry & Medicine. The author has an hindex of 3, co-authored 4 publications.
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Papers
Natural deep eutectic solvents as an efficient and reusable active system for the Nazarov cyclization
Stefano Nejrotti,Marta Iannicelli,Salwa Simona Jamil,Davide Arnodo,Marco Blangetti,Cristina Prandi +5 more
TL;DR: In this article, the Nazarov cyclization of divinyl ketones to obtain cyclopentenones has been investigated in deep eutectic solvents for an increasing number of synthetic transformations.
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Lateral lithiation in deep eutectic solvents: regioselective functionalization of substituted toluene derivatives
TL;DR: The heteroatom-directed lateral lithiation of functionalized toluenes in a choline chloride-based eutectic mixture is reported, providing a rapid and high regioselective access to functionalized aromatic derivatives of remarkable synthetic value.
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Combination of Enzymes and Deep Eutectic Solvents as Powerful Toolbox for Organic Synthesis
TL;DR: In this article , a review aims to show the newly reported protocols in the field, subdivided by reaction class as a 'toolbox' guide for organic synthesis, as an improvement in terms of selectivity and sustainability.
Deep eutectic solvents as H2-sources for Ru(II)-catalyzed transfer hydrogenation of carbonyl compounds under mild conditions
Marzia Cavallo,Davide Arnodo,Alberto Mannu,Marco Blangetti,Cristina Prandi,Walter Baratta,Salvatore Baldino +6 more
TL;DR: In this article, the authors employed ruthenium(II)-complexes as pre-catalysts in the transfer hydrogenation of carbonyl compounds in deep eutectic media.
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From oximes to tertiary alcohols in water, at room temperature and under air: a hybrid one-pot tandem assembly of enzymatic deoximation and RLi/RMgX reagents.
Davide Arnodo,Marina Ramos-Martín,Luciana Cicco,Vito Capriati,Nicolás Ríos-Lombardía,Javier González-Sabín,Alejandro Presa Soto,Joaquín García-Álvarez +7 more
TL;DR: In this paper , the highly efficient biodeoximation of aromatic ketoximes, promoted by the enzymatic oxidative system laccase/TEMPO/O2, has been successfully assembled with the fast and chemoselective addition of highly-polar s-block organometallic reagents (RLi/RMgX) en route to highlysubstituted tertiary alcohols.
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