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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.

DOI:10.3762/bjoc.17.32
PMID:33828616
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7871035/
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。

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Quest for a Symmetric [C-F-C] Fluoronium Ion in Solution: A Winding Path to Ultimate Success.
Formation of synthetically relevant CF-substituted phenonium ions in superacid media.
在超酸介质中形成具有合成相关性的含氟取代苯鎓离子。
RSC Adv. 2021 Jul 26;11(41):25695-25699. doi: 10.1039/d1ra04901a. eCollection 2021 Jul 19.
在溶液中探索对称的 [C-F-C] 氟翁离子:通向最终成功的曲折道路。
Acc Chem Res. 2020 Jan 21;53(1):265-275. doi: 10.1021/acs.accounts.9b00554. Epub 2019 Dec 26.
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Catalytic Synthesis of Trifluoromethylated Allenes, Indenes, Chromenes, and Olefins from Propargylic Alcohols in HFIP.在六氟异丙醇中由炔丙醇催化合成三氟甲基化丙二烯、茚、色烯和烯烃。
J Org Chem. 2019 Dec 20;84(24):15926-15947. doi: 10.1021/acs.joc.9b02398. Epub 2019 Dec 4.
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The cyclopropylcarbinyl route to γ-silyl carbocations.通往γ-硅基碳正离子的环丙基甲基路线。
Beilstein J Org Chem. 2019 Jul 24;15:1769-1780. doi: 10.3762/bjoc.15.170. eCollection 2019.
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Ga(OTf)-Catalyzed Temperature-Controlled Regioselective Friedel-Crafts Alkylation of Trifluoromethylated 3-Indolylmethanols with 2-Substituted Indoles: Divergent Synthesis of Trifluoromethylated Unsymmetrical 3,3'-and 3,6'-Bis(indolyl)methanes.三氟甲磺酸镓催化的三氟甲基化3-吲哚甲醇与2-取代吲哚的温度控制区域选择性傅克烷基化反应:三氟甲基化不对称3,3'-和3,6'-双(吲哚基)甲烷的发散合成
Org Lett. 2019 May 3;21(9):3396-3401. doi: 10.1021/acs.orglett.9b01135. Epub 2019 Apr 22.
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Carbene-Catalyzed Enantioselective Decarboxylative Annulations to Access Dihydrobenzoxazinones and Quinolones.卡宾催化的对映选择性脱羧环化反应构建二氢苯并恶嗪酮和喹诺酮。
Angew Chem Int Ed Engl. 2019 Apr 23;58(18):5941-5945. doi: 10.1002/anie.201900600. Epub 2019 Mar 27.
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Catalytic Geminal Difluorination of Styrenes for the Construction of Fluorine-rich Bioisosteres.用于构建富含氟生物电子等排体的苯乙烯催化偕二氟烷基化反应
Org Lett. 2018 Dec 21;20(24):8073-8076. doi: 10.1021/acs.orglett.8b03794. Epub 2018 Dec 11.
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The Experimental Evidence in Support of Glycosylation Mechanisms at the S1-S2 Interface.支持 S1-S2 界面糖基化机制的实验证据。
Chem Rev. 2018 Sep 12;118(17):8242-8284. doi: 10.1021/acs.chemrev.8b00083. Epub 2018 May 30.
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Asymmetric nucleophilic fluorination under hydrogen bonding phase-transfer catalysis.氢键相转移催化下的不对称亲核氟化反应。
Science. 2018 May 11;360(6389):638-642. doi: 10.1126/science.aar7941.