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Chemoselective Hydrogenation of alpha,beta-Unsaturated Carbonyls Catalyzed by Biomass-Derived Cobalt Nanoparticles in Water

机译:在水中生物质衍生的钴纳米粒子催化的α,β-不饱和羰基的化学选择氢化

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摘要

Herein, we report highly chemoselective hydrogenation of alpha,beta-unsaturated carbonyls to saturated carbonyls catalyzed by cobalt nanoparticles supported on the biomass-derived carbon from bamboo shoots with molecular hydrogen in water, which is the first prototype using a heterogeneous non-noble metal catalyst for such organic transformation as far as we know. The optimal cobalt nanocatalyst, CoOx@NC-800, manifested remarkable activity and selectivity for hydrogenation of C=C in alpha,beta-unsaturated carbonyls under mild conditions. A broad set of alpha,beta-aromatic and aliphatic unsaturated carbonyls were selectively reduced to their corresponding saturated carbonyls in up to 99 % yields with good tolerance of various functional groups. Meanwhile, a new straightforward one-pot cascade synthesis of saturated carbonyls was realized with high activity and selectivity via the cross-aldol condensation of ketones with aldehydes followed by selective hydrogenation. More importantly, this one-pot strategy is applicable for the expedient synthesis of Loureirin A, a versatile bioactive and medicinal molecule, from readily available starting materials, further highlighting the practical utility of the catalyst. In addition, the catalyst can be easily separated for successive reuses without significant loss in both activity and selectivity.
机译:在此,我们报告了通过在水中分子氢的分子氢的竹笋上负载的钴纳米粒子催化的α,β-不饱和羰基对饱和碳基的高度化学溶解至饱和羰基,这是使用异质非贵金属催化剂的第一原型对于我们所知道的这种有机转变。最佳的钴纳米催化剂,CoOX @ NC-800,在温和条件下α,β-不饱和羰基氢化的显着活性和选择性C = C.将宽α,β-芳族和脂族不饱和羰基选择性地减少至其相应的饱和羰基,高达99%的产率,其具有良好的各种官能团的耐受性。同时,通过高活性和选择性通过丙酮与醛接合选择性氢化,以高活性和选择性实现饱和羰基的新的直接的单壶级联合成。更重要的是,这种单罐策略适用于洛氏林A,多功能生物活性和药物分子的权宜之计,从易于获得的原料中进一步突出催化剂的实用效用。此外,催化剂可以容易地分离成连续的重复速度,而无需缺两种活性和选择性。

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