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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...

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Autores principales: Lansbergen, Beatrice, Granatino, Paola, Ritter, Tobias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
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.
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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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