首页> 外文期刊>Canadian Journal of Chemistry >Highly stereoselective facile synthesis of β-amino carbonyl compounds via a Mannich-type reaction catalyzed by γ-AI2O3/MeSO3H (alumina/methanesulfonic acid: AMA) as a recyclable, efficient, and versatile heterogeneous catalyst
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Highly stereoselective facile synthesis of β-amino carbonyl compounds via a Mannich-type reaction catalyzed by γ-AI2O3/MeSO3H (alumina/methanesulfonic acid: AMA) as a recyclable, efficient, and versatile heterogeneous catalyst

机译:通过γ-Al2O3/ MeSO3H(氧化铝/甲磺酸:AMA)催化的曼尼希型反应,高度立体选择性地合成β-氨基羰基化合物,这是一种可循环利用,高效且用途广泛的多相催化剂

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摘要

Mannich reaction of ketones, aromatic aldehydes, and aromatic amines catalyzed efficiently by γ-AbOs/MeSCbH (aluimna/methanesulfonic acid: AMA) as a heterogeneous catalyst, which were carried out in EtOH at ambient temperature to afford the corresponding β-amino ketones in good yields and high stereoselectivities in favor of the anti isomer, was described for the first time. It was found that this catalyst could be completely recovered and reused without loss of its catalytic activities and is thus environmentally conscious. Furthermore, the use of γ-AI2O3/CH3SO3H (AMA) catalyst is feasible because of its easy preparation, easy handling, stability, easy recovery, reusability, good activity, stereoselectivity, and eco-friendliness. The use of this method provides a novel and improved modification of the three-component Mannich reaction in terms of mild reaction conditions and clean reaction profiles, using a very small quantity of catalyst and a simple workup procedure.
机译:γ-AbOs/ MeSCbH(铝/甲磺酸:AMA)作为多相催化剂有效催化酮,芳族醛和芳族胺的曼尼希反应,在环境温度下于EtOH中进行反应,得到相应的β-氨基酮首次描述了有利于抗异构体的高收率和高立体选择性。发现该催化剂可以完全回收和再利用而不会损失其催化活性,因此具有环保意识。此外,使用γ-Al2 O 3 / CH 3 SO 3 H(AMA)催化剂是可行的,因为它易于制备,易于处理,稳定,易于回收,可重复使用,活性好,立体选择性和环保。该方法的使用,在温和的反应条件和干净的反应曲线方面,使用了很少量的催化剂和简单的后处理程序,就对三组分曼尼希反应进行了新颖和改进的改进。

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