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铁催化的酮酸与脂肪醛的断裂反应在酮和酮酯的合成中的应用。

Iron-Catalyzed Cleavage Reaction of Keto Acids with Aliphatic Aldehydes for the Synthesis of Ketones and Ketone Esters.

机构信息

The Key Laboratory of Environmentally Friendly Chemistry and Application of the Ministry of Education, The Key Laboratory for Green Organic Synthesis and Application of Hunan Province, College of Chemistry, Xiangtan University, Xiangtan, 411105, P. R. China.

College of Science, Hunan Agricultural University, Changsha, 410128, P. R. China.

出版信息

Chemistry. 2020 Apr 1;26(19):4246-4250. doi: 10.1002/chem.202000114. Epub 2020 Mar 3.

Abstract

The radical-radical coupling reaction is an important synthetic strategy. In this study, the iron-catalyzed radical-radical cross-coupling reaction based on the decarboxylation of keto acids and decarbonylation of aliphatic aldehydes to obtain valuable aryl ketones is reported for the first time. Remarkably, when tertiary aldehydes were used as carbonyl sources, ketone esters were selectively obtained instead of ketones. The gram-scale preparation of aryl ketone through this strategy was easily achieved by using only 3 mol % of the iron catalyst. As a proof-of-concept, the bioactive molecule flurprimidol was synthesized in two steps by using this strategy.

摘要

自由基-自由基偶联反应是一种重要的合成策略。在这项研究中,首次报道了基于酮酸脱羧和脂肪醛脱羰的铁催化自由基-自由基交叉偶联反应,以获得有价值的芳基酮。值得注意的是,当使用叔醛作为羰基源时,选择性地得到酮酯而不是酮。通过该策略,仅使用 3 mol%的铁催化剂即可轻松实现芳基酮的克级制备。作为概念验证,通过该策略两步合成了生物活性分子氟啶菌胺。

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