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咪唑衍生物在使用甲酸盐的钌催化烯烃水酯交换反应中取得显著改进。

Remarkable improvement achieved by imidazole derivatives in ruthenium-catalyzed hydroesterification of alkenes using formates.

机构信息

School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Shizuoka 422-8526, Japan.

出版信息

Org Lett. 2012 Sep 21;14(18):4722-5. doi: 10.1021/ol301850y. Epub 2012 Aug 30.

Abstract

Imidazole derivatives are revealed to be effective ligands in the Ru-catalyzed hydroesterification of alkenes using formates, affording one-carbon-elongated esters in high yields. Further, intramolecular hydroesterification was successfully performed to give lactones for the first time. Imidazole derivatives can contribute to promote the reaction as well as to suppress the undesired decarbonylation of formate. Toxic CO gas, a directing group, and large excess alkenes are not required.

摘要

咪唑衍生物被证明是 Ru 催化的使用甲酸盐的烯烃氢酯化反应中的有效配体,以高产率提供了一碳延长的酯。此外,首次成功地进行了分子内氢酯化反应,得到了内酯。咪唑衍生物不仅可以促进反应,还可以抑制甲酸盐的不希望的脱羧反应。不需要有毒的 CO 气体、导向基团和大量过量的烯烃。

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