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C4–H indole functionalisation: precedent and prospects

C4-decorated indoles feature in a plethora of bioactive and functional compounds of importance to natural product synthesis, material sciences, as well as crop protection and pharmaceutical industries. Traditionally, their syntheses largely involved harsh stoichiometric metalations and radical react...

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Detalles Bibliográficos
Autores principales: Kalepu, Jagadeesh, Gandeepan, Parthasarathy, Ackermann, Lutz, Pilarski, Lukasz T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944383/
https://www.ncbi.nlm.nih.gov/pubmed/29780550
http://dx.doi.org/10.1039/c7sc05336c
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author Kalepu, Jagadeesh
Gandeepan, Parthasarathy
Ackermann, Lutz
Pilarski, Lukasz T.
author_facet Kalepu, Jagadeesh
Gandeepan, Parthasarathy
Ackermann, Lutz
Pilarski, Lukasz T.
author_sort Kalepu, Jagadeesh
collection PubMed
description C4-decorated indoles feature in a plethora of bioactive and functional compounds of importance to natural product synthesis, material sciences, as well as crop protection and pharmaceutical industries. Traditionally, their syntheses largely involved harsh stoichiometric metalations and radical reactions. However, transition metal catalysed C–H activation has recently evolved into a powerful strategy for the late-stage diversification of indoles at the C4–H position. Modern photoredox, enzymatic and precious transition metal catalysis represent the key stimuli for developing challenging C–C and C–Het bond forming transformations under mild reaction conditions. Herein, we discuss the evolution and application of these methods for the step-economical transformations of otherwise inert C4–H bonds up to December 2017.
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spelling pubmed-59443832018-05-18 C4–H indole functionalisation: precedent and prospects Kalepu, Jagadeesh Gandeepan, Parthasarathy Ackermann, Lutz Pilarski, Lukasz T. Chem Sci Chemistry C4-decorated indoles feature in a plethora of bioactive and functional compounds of importance to natural product synthesis, material sciences, as well as crop protection and pharmaceutical industries. Traditionally, their syntheses largely involved harsh stoichiometric metalations and radical reactions. However, transition metal catalysed C–H activation has recently evolved into a powerful strategy for the late-stage diversification of indoles at the C4–H position. Modern photoredox, enzymatic and precious transition metal catalysis represent the key stimuli for developing challenging C–C and C–Het bond forming transformations under mild reaction conditions. Herein, we discuss the evolution and application of these methods for the step-economical transformations of otherwise inert C4–H bonds up to December 2017. Royal Society of Chemistry 2018-04-20 /pmc/articles/PMC5944383/ /pubmed/29780550 http://dx.doi.org/10.1039/c7sc05336c Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Kalepu, Jagadeesh
Gandeepan, Parthasarathy
Ackermann, Lutz
Pilarski, Lukasz T.
C4–H indole functionalisation: precedent and prospects
title C4–H indole functionalisation: precedent and prospects
title_full C4–H indole functionalisation: precedent and prospects
title_fullStr C4–H indole functionalisation: precedent and prospects
title_full_unstemmed C4–H indole functionalisation: precedent and prospects
title_short C4–H indole functionalisation: precedent and prospects
title_sort c4–h indole functionalisation: precedent and prospects
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944383/
https://www.ncbi.nlm.nih.gov/pubmed/29780550
http://dx.doi.org/10.1039/c7sc05336c
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