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Site-Selective C–H alkylation of Complex Arenes by a Two-Step Aryl Thianthrenation-Reductive Alkylation Sequence
[Image: see text] Herein, we present an undirected para-selective two-step C–H alkylation of complex arenes useful for late-stage functionalization. The combination of a site-selective C–H thianthrenation with palladium-catalyzed reductive electrophile cross-coupling grants access to a diverse range...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8297726/ https://www.ncbi.nlm.nih.gov/pubmed/34028272 http://dx.doi.org/10.1021/jacs.1c03459 |
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author | Lansbergen, Beatrice Granatino, Paola Ritter, Tobias |
author_facet | Lansbergen, Beatrice Granatino, Paola Ritter, Tobias |
author_sort | Lansbergen, Beatrice |
collection | PubMed |
description | [Image: see text] Herein, we present an undirected para-selective two-step C–H alkylation of complex arenes useful for late-stage functionalization. The combination of a site-selective C–H thianthrenation with palladium-catalyzed reductive electrophile cross-coupling grants access to a diverse range of synthetically useful alkylated arenes which cannot be accessed otherwise with comparable selectivity, diversity, and practicality. The robustness of this transformation is further demonstrated by thianthrenium-based reductive coupling of two complex fragments. |
format | Online Article Text |
id | pubmed-8297726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82977262021-07-23 Site-Selective C–H alkylation of Complex Arenes by a Two-Step Aryl Thianthrenation-Reductive Alkylation Sequence Lansbergen, Beatrice Granatino, Paola Ritter, Tobias J Am Chem Soc [Image: see text] Herein, we present an undirected para-selective two-step C–H alkylation of complex arenes useful for late-stage functionalization. The combination of a site-selective C–H thianthrenation with palladium-catalyzed reductive electrophile cross-coupling grants access to a diverse range of synthetically useful alkylated arenes which cannot be accessed otherwise with comparable selectivity, diversity, and practicality. The robustness of this transformation is further demonstrated by thianthrenium-based reductive coupling of two complex fragments. American Chemical Society 2021-05-24 2021-06-02 /pmc/articles/PMC8297726/ /pubmed/34028272 http://dx.doi.org/10.1021/jacs.1c03459 Text en © 2021 The Authors. Published by American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Lansbergen, Beatrice Granatino, Paola Ritter, Tobias Site-Selective C–H alkylation of Complex Arenes by a Two-Step Aryl Thianthrenation-Reductive Alkylation Sequence |
title | Site-Selective
C–H alkylation of Complex Arenes
by a Two-Step Aryl Thianthrenation-Reductive Alkylation Sequence |
title_full | Site-Selective
C–H alkylation of Complex Arenes
by a Two-Step Aryl Thianthrenation-Reductive Alkylation Sequence |
title_fullStr | Site-Selective
C–H alkylation of Complex Arenes
by a Two-Step Aryl Thianthrenation-Reductive Alkylation Sequence |
title_full_unstemmed | Site-Selective
C–H alkylation of Complex Arenes
by a Two-Step Aryl Thianthrenation-Reductive Alkylation Sequence |
title_short | Site-Selective
C–H alkylation of Complex Arenes
by a Two-Step Aryl Thianthrenation-Reductive Alkylation Sequence |
title_sort | site-selective
c–h alkylation of complex arenes
by a two-step aryl thianthrenation-reductive alkylation sequence |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8297726/ https://www.ncbi.nlm.nih.gov/pubmed/34028272 http://dx.doi.org/10.1021/jacs.1c03459 |
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