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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Highly efficient selective oxidation of alcohols to carbonyl compounds catalyzed by ruthenium (III) meso-tetraphenylporphyrin chloride in the presence of molecular oxygen.
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Highly efficient selective oxidation of alcohols to carbonyl compounds catalyzed by ruthenium (III) meso-tetraphenylporphyrin chloride in the presence of molecular oxygen.

机译:在分子氧存在下,钌(III)内-四苯基卟啉氯化物催化的醇高效选择性氧化为羰基化合物。

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摘要

Efficient selective oxidation of alcohols to carbonyl compounds by molecular oxygen with isobutyraldehyde as oxygen acceptor in the presence of metalloporphyrins has been reported. Ruthenium (III) meso-tetraphenylporphyrin chloride (Ru(TPP)Cl) showed excellent activity and selectivity for oxidation of various alcohols under mild conditions. Moreover, different factors influencing alcohols oxidation, for example, catalyst, solvent, temperature, and oxidant, have been investigated. In large-scale oxidation of benzyl alcohol, the isolated yield of benzaldehyde of 89% was observed.
机译:已经报道了在金属卟啉存在下,用异丁醛作为氧受体通过分子氧将醇有效地选择性氧化为羰基化合物。钌(III)内四苯基卟啉氯化物(Ru(TPP)Cl)在温和的条件下显示出优异的活性和对各种醇氧化的选择性。而且,已经研究了影响醇氧化的不同因素,例如催化剂,溶剂,温度和氧化剂。在苯甲醇的大规模氧化中,苯甲醛的分离产率为89%。

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