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Article dans une revue

Photocatalytic Radical Addition to Levoglucosenone

Abstract : Using photocatalysis with tetra-n-butylammonium decatungstate (TBADT), alkanes, cyclic acetals, cyclic ethers, formamide and aldehydes were added in a stereoselective way to levoglucosenone (LGO). A hydrogen atom is transferred from the donor compound to the photochemically excited TBADT, and the resulting radicals add onto LGO in a stereoselective way. In the case of the addition of adamantane, two regioisomers were obtained which form a crystalline solid solution. Cyrene™, obtained by hydrogenation of LGO, was added under the same conditions. In this case, only two of 32 possible isomers of the resulting Cyrene™ dimer were formed. The regio-selectivity of the HAT step is discussed in detail. For this purpose, bond dissociation energies and partial charges have been calculated. Transition state calculations of the radical addition to LGO explain the stereospecificity of this reaction step.
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Soumis le : vendredi 7 janvier 2022 - 10:45:34
Dernière modification le : mardi 18 janvier 2022 - 17:06:16


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Corentin Lefebvre, Terence van Gysel, Clément Michelin, Elodie Rousset, Djibril Djiré, et al.. Photocatalytic Radical Addition to Levoglucosenone. European Journal of Organic Chemistry, Wiley-VCH Verlag, 2022, 2022 (1), pp.e202101298. ⟨10.1002/ejoc.202101298⟩. ⟨hal-03499878v2⟩



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