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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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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. |
format | Online Article Text |
id | pubmed-5944383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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