Abstract
Esters containing tertiary amine functionalities were successfully synthesized under mild conditions and in good yields, using a three-step process involving the activation of acids into their corresponding cyanomethyl esters, followed by transesterification with the alcohol counterparts, and subsequent scavenging of the excess of alcohol to facilitate purification. © 2009 Elsevier Ltd. All rights reserved.
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Bouillon, C., Quéléver, G., & Peng, L. (2009). Efficient synthesis of esters containing tertiary amine functionalities via active cyanomethyl ester intermediates. Tetrahedron Letters, 50(30), 4346–4349. https://doi.org/10.1016/j.tetlet.2009.05.034
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