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通过 Oxone 催化的羧酸和醇的脱氢反应高效合成酯。

Efficient synthesis of esters through oxone-catalyzed dehydrogenation of carboxylic acids and alcohols.

机构信息

College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou, Gansu 730070, People's Republic of China.

出版信息

Org Biomol Chem. 2018 Dec 12;16(48):9472-9476. doi: 10.1039/c8ob02539h.

DOI:10.1039/c8ob02539h
PMID:30516792
Abstract

Since esters are important organic synthesis intermediates, an environmentally friendly oxone catalyzed-esterification of carboxylic acids with alcohols has been developed. A series of carboxylic acid esters are obtained in high yield. This strategy requires mild reaction conditions, providing an attractive alternative for the construction of valuable carbonyl esters. Electron-rich and electron-deficient groups are compatible with the standard conditions and a variety of substrates are demonstrated. Moreover, the reaction could easily be adapted to typical prodrugs, drugs and gram-scale synthesis.

摘要

由于酯类是重要的有机合成中间体,因此开发了一种绿色环保的过氧单硫酸盐催化羧酸与醇的酯化反应。该方法可以高产率得到一系列羧酸酯。该策略所需的反应条件温和,为构建有价值的羰基酯提供了一种有吸引力的替代方法。富电子和缺电子基团与标准条件兼容,并且可以证明多种底物适用。此外,该反应可以很容易地适用于典型的前药、药物和克级规模的合成。

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