Cargando…

CF(3)-substituted carbocations: underexploited intermediates with great potential in modern synthetic chemistry

“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...

Descripción completa

Detalles Bibliográficos
Autores principales: Fernandes, Anthony J, Panossian, Armen, Michelet, Bastien, Martin-Mingot, Agnès, Leroux, Frédéric R, Thibaudeau, Sébastien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871035/
https://www.ncbi.nlm.nih.gov/pubmed/33828616
http://dx.doi.org/10.3762/bjoc.17.32
_version_ 1783648933443010560
author Fernandes, Anthony J
Panossian, Armen
Michelet, Bastien
Martin-Mingot, Agnès
Leroux, Frédéric R
Thibaudeau, Sébastien
author_facet Fernandes, Anthony J
Panossian, Armen
Michelet, Bastien
Martin-Mingot, Agnès
Leroux, Frédéric R
Thibaudeau, Sébastien
author_sort Fernandes, Anthony J
collection PubMed
description “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(3)-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.
format Online
Article
Text
id pubmed-7871035
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Beilstein-Institut
record_format MEDLINE/PubMed
spelling pubmed-78710352021-04-06 CF(3)-substituted carbocations: underexploited intermediates with great potential in modern synthetic chemistry Fernandes, Anthony J Panossian, Armen Michelet, Bastien Martin-Mingot, Agnès Leroux, Frédéric R Thibaudeau, Sébastien Beilstein J Org Chem Review “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(3)-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. Beilstein-Institut 2021-02-03 /pmc/articles/PMC7871035/ /pubmed/33828616 http://dx.doi.org/10.3762/bjoc.17.32 Text en Copyright © 2021, Fernandes et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/terms/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the author(s) and source are credited and that individual graphics may be subject to special legal provisions. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms/terms)
spellingShingle Review
Fernandes, Anthony J
Panossian, Armen
Michelet, Bastien
Martin-Mingot, Agnès
Leroux, Frédéric R
Thibaudeau, Sébastien
CF(3)-substituted carbocations: underexploited intermediates with great potential in modern synthetic chemistry
title CF(3)-substituted carbocations: underexploited intermediates with great potential in modern synthetic chemistry
title_full CF(3)-substituted carbocations: underexploited intermediates with great potential in modern synthetic chemistry
title_fullStr CF(3)-substituted carbocations: underexploited intermediates with great potential in modern synthetic chemistry
title_full_unstemmed CF(3)-substituted carbocations: underexploited intermediates with great potential in modern synthetic chemistry
title_short CF(3)-substituted carbocations: underexploited intermediates with great potential in modern synthetic chemistry
title_sort cf(3)-substituted carbocations: underexploited intermediates with great potential in modern synthetic chemistry
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871035/
https://www.ncbi.nlm.nih.gov/pubmed/33828616
http://dx.doi.org/10.3762/bjoc.17.32
work_keys_str_mv AT fernandesanthonyj cf3substitutedcarbocationsunderexploitedintermediateswithgreatpotentialinmodernsyntheticchemistry
AT panossianarmen cf3substitutedcarbocationsunderexploitedintermediateswithgreatpotentialinmodernsyntheticchemistry
AT micheletbastien cf3substitutedcarbocationsunderexploitedintermediateswithgreatpotentialinmodernsyntheticchemistry
AT martinmingotagnes cf3substitutedcarbocationsunderexploitedintermediateswithgreatpotentialinmodernsyntheticchemistry
AT lerouxfredericr cf3substitutedcarbocationsunderexploitedintermediateswithgreatpotentialinmodernsyntheticchemistry
AT thibaudeausebastien cf3substitutedcarbocationsunderexploitedintermediateswithgreatpotentialinmodernsyntheticchemistry