新型l -丝氨酸衍生物配体作为diels-alder反应的助催化剂。

ISRN Organic Chemistry Pub Date : 2013-12-05 eCollection Date: 2013-01-01 DOI:10.1155/2013/217675
Carlos A D Sousa, José E Rodríguez-Borges, Cristina Freire
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引用次数: 4

摘要

制备了新的l -丝氨酸衍生物配体,并在几种路易斯酸存在下,作为环戊二烯(CPD)与丙烯酸甲酯的Diels-Alder反应的助催化剂。根据反应产率评价了原位形成的配合物的催化潜力。双齿丝氨酸配体对中等强度路易斯酸具有良好的配位能力,从而提高了其催化活性。结果表明,l -丝氨酸配体的合成高效、简便。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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New L-serine derivative ligands as cocatalysts for diels-alder reaction.

New L-serine derivative ligands were prepared and tested as cocatalyst in the Diels-Alder reactions between cyclopentadiene (CPD) and methyl acrylate, in the presence of several Lewis acids. The catalytic potential of the in situ formed complexes was evaluated based on the reaction yield. Bidentate serine ligands showed good ability to coordinate medium strength Lewis acids, thus boosting their catalytic activity. The synthesis of the L-serine ligands proved to be highly efficient and straightforward.

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