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铁催化末端炔烃与过氧烷基化合物的自由基脱羧氧烷基化反应。

Iron-Catalyzed Radical Decarboxylative Oxyalkylation of Terminal Alkynes with Alkyl Peroxides.

机构信息

Key Laboratory of Coal to Ethylene Glycol and Its Related Technology, State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, University of Chinese Academy of Sciences, 155 Yangqiao Road West, Fuzhou, Fujian, 350002, P. R. China.

出版信息

Chemistry. 2017 Aug 1;23(43):10254-10258. doi: 10.1002/chem.201701830. Epub 2017 Jul 6.

Abstract

An iron-catalyzed oxyalkylation of alkynes with alkyl peroxides as the alkylating reagents has been investigated. Alkyl peroxides are readily available from aliphatic acids and serve simultaneously as the alkylating reagents and internal oxidants. Primary, secondary, and tertiary alkyl groups of aliphatic acids were readily incorporated into C-C triple bonds and diverse α-alkylated ketones were synthesized. Mechanism studies revealed that this reaction involves highly reactive alkyl free radicals. A unique equilibrium between lauric acid and water catalyzed by the iron(III) catalyst was observed.

摘要

一种铁催化的炔烃与过氧烷基化合物的氧烷基化反应已经被研究。过氧烷基化合物可从脂肪酸中轻易获得,同时作为烷基化试剂和内部氧化剂。脂肪酸的伯、仲和叔烷基很容易与 C-C 三键结合,合成了多种α-烷基化酮。机理研究表明,该反应涉及高活性的烷基自由基。通过铁(III)催化剂催化观察到一种独特的月桂酸和水之间的平衡。

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