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含氟取代的碳正离子:现代合成化学中未被充分利用但具有巨大潜力的中间体。

CF-substituted carbocations: underexploited intermediates with great potential in modern synthetic chemistry.

作者信息

Fernandes Anthony J, Panossian Armen, Michelet Bastien, Martin-Mingot Agnès, Leroux Frédéric R, Thibaudeau Sébastien

机构信息

Université de Strasbourg, Université de Haute-Alsace, CNRS, UMR 7042-LIMA, ECPM, 25 Rue Becquerel, 67087 Strasbourg, France.

Université de Poitiers, CNRS, IC2MP, UMR 7285, Equipe "Synthèse Organique", 4 Rue Michel Brunet, 86073 Poitiers Cedex 9, France.

出版信息

Beilstein J Org Chem. 2021 Feb 3;17:343-378. doi: 10.3762/bjoc.17.32. eCollection 2021.

Abstract

"The extraordinary instability of such an "ion" accounts for many of the peculiarities of organic reactions" - Franck C. Whitmore (1932). This statement from Whitmore came in a period where carbocations began to be considered as intermediates in reactions. Ninety years later, pointing at the strong knowledge acquired from the contributions of famous organic chemists, carbocations are very well known reaction intermediates. Among them, destabilized carbocations - carbocations substituted with electron-withdrawing groups - are, however, still predestined to be transient species and sometimes considered as exotic ones. Among them, the CF-substituted carbocations, frequently suggested to be involved in synthetic transformations but rarely considered as affordable intermediates for synthetic purposes, have long been investigated. This review highlights recent and past reports focusing on their study and potential in modern synthetic transformations.

摘要

“这种‘离子’的异常不稳定性解释了有机反应的许多特性”——弗兰克·C·惠特莫尔(1932年)。惠特莫尔的这一表述出现在碳正离子开始被视为反应中间体的时期。九十年后,鉴于从著名有机化学家的贡献中所获得的丰富知识,碳正离子已是广为人知的反应中间体。然而,在它们之中,不稳定的碳正离子——被吸电子基团取代的碳正离子——仍然注定是瞬态物种,有时还被视为奇特的物种。其中,经常被认为参与合成转化但很少被视为适合合成用途的中间体的CF取代碳正离子,长期以来一直受到研究。本综述重点介绍了近期和过去关于它们的研究以及在现代合成转化中的潜力的报告。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/509d/7871035/15bf66d0c145/Beilstein_J_Org_Chem-17-343-g002.jpg

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