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胺催化的β-酮羧酸与三氟丙酮酸的脱羧醛醇缩合反应。

Amine-Catalyzed Decarboxylative Aldol Reaction of β-Ketocarboxylic Acids with Trifluoropyruvates.

机构信息

Department of Applied Chemistry and Life Science, Toyohashi University of Technology, 1-1 Hibarigaoka, Tempaku-cho, Toyohashi 441-8580, Japan.

出版信息

Molecules. 2019 Jul 30;24(15):2773. doi: 10.3390/molecules24152773.

Abstract

Decarboxylative aldol reaction of aliphatic carboxylic acids is a useful method for C-C bond formation because carboxylic acids are an easily available class of compounds. In this study, we found that the decarboxylative aldol reaction of tertiary β-ketocarboxylic acids and trifluoropyruvates proceeded smoothly to yield the corresponding aldol products in high yields and with high diastereoselectivity in the presence of a tertiary amine catalyst. In this reaction, we efficiently constructed a quaternary carbon center and an adjacent trifluoromethylated carbon center. This protocol was also extended to an enantioselective reaction with a chiral amine catalyst, and the desired product was obtained with up to 73% enantioselectivity.

摘要

脂肪族羧酸的脱羧醛缩合反应是一种有用的 C-C 键形成方法,因为羧酸是一类易于获得的化合物。在这项研究中,我们发现,在叔胺催化剂的存在下,叔β-酮羧酸和三氟丙酮酸的脱羧醛缩合反应顺利进行,以高产率和高非对映选择性得到相应的醛缩产物。在该反应中,我们有效地构建了一个季碳原子和一个相邻的三氟甲基化的碳原子。该方案也被扩展到使用手性胺催化剂的对映选择性反应中,并用高达 73%的对映选择性获得了所需的产物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c542/6695914/72382452d234/molecules-24-02773-g001.jpg

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