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- W2896286499 abstract "A combination of aryl diselenides/hydrogen peroxide and carbon-nanotube/rhodium nanohybrids for naphthol oxidation is reported. The synthesis of 1,4-naphthoquinones and evaluation of their relevant trypanocidal activity was accomplished in an elegant manner. Several benzenoid (A-ring)-substituted quinones are described, prepared in moderate to high yields. The synthesis of A-ring-substituted 1,4-naphthoquinones is a challenge. The contribution of carbon-nanotube/Rh as co-catalyst in this process was investigated and, in some cases, yields were improved. This method provides an efficient and versatile alternative for preparing A-ring-modified naphthoquinonoid compounds with relevant biological profiles. More information can be found in the Full Paper by E. Doris, E. N. da Silva Júnior, et al. on page 15227. A combination of aryl diselenides/hydrogen peroxide and carbon-nanotube/rhodium nanohybrids for naphthol oxidation is reported. The synthesis of 1,4-naphthoquinones and evaluation of their relevant trypanocidal activity was accomplished in an elegant manner. Several benzenoid (A-ring)-substituted quinones are described, prepared in moderate to high yields. The synthesis of A-ring-substituted 1,4-naphthoquinones is a challenge. The contribution of carbon-nanotube/Rh as co-catalyst in this process was investigated and, in some cases, yields were improved. This method provides an efficient and versatile alternative for preparing A-ring-modified naphthoquinonoid compounds with relevant biological profiles. More information can be found in the Full Paper by E. Doris, E. N. da Silva Júnior, et al. on page 15227." @default.
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- W2896286499 date "2018-09-06" @default.
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- W2896286499 title "Front Cover: Combination of Aryl Diselenides/Hydrogen Peroxide and Carbon‐Nanotube/Rhodium Nanohybrids for Naphthol Oxidation: An Efficient Route towards Trypanocidal Quinones (Chem. Eur. J. 57/2018)" @default.
- W2896286499 doi "https://doi.org/10.1002/chem.201803537" @default.
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