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Modular allylation of C(sp(3))–H bonds by combining decatungstate photocatalysis and HWE olefination in flow

The late-stage introduction of allyl groups provides an opportunity to synthetic organic chemists for subsequent diversification, furnishing a rapid access to new chemical space. Here, we report the development of a modular synthetic sequence for the allylation of strong aliphatic C(sp(3))–H bonds....

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Autores principales: Capaldo, Luca, Bonciolini, Stefano, Pulcinella, Antonio, Nuño, Manuel, Noël, Timothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214841/
https://www.ncbi.nlm.nih.gov/pubmed/35799818
http://dx.doi.org/10.1039/d2sc01581a
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author Capaldo, Luca
Bonciolini, Stefano
Pulcinella, Antonio
Nuño, Manuel
Noël, Timothy
author_facet Capaldo, Luca
Bonciolini, Stefano
Pulcinella, Antonio
Nuño, Manuel
Noël, Timothy
author_sort Capaldo, Luca
collection PubMed
description The late-stage introduction of allyl groups provides an opportunity to synthetic organic chemists for subsequent diversification, furnishing a rapid access to new chemical space. Here, we report the development of a modular synthetic sequence for the allylation of strong aliphatic C(sp(3))–H bonds. Our sequence features the merger of two distinct steps to accomplish this goal, including a photocatalytic Hydrogen Atom Transfer and an ensuing Horner–Wadsworth–Emmons (HWE) reaction. This practical protocol enables the modular and scalable allylation of valuable building blocks and has been applied to structurally complex molecules.
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spelling pubmed-92148412022-07-06 Modular allylation of C(sp(3))–H bonds by combining decatungstate photocatalysis and HWE olefination in flow Capaldo, Luca Bonciolini, Stefano Pulcinella, Antonio Nuño, Manuel Noël, Timothy Chem Sci Chemistry The late-stage introduction of allyl groups provides an opportunity to synthetic organic chemists for subsequent diversification, furnishing a rapid access to new chemical space. Here, we report the development of a modular synthetic sequence for the allylation of strong aliphatic C(sp(3))–H bonds. Our sequence features the merger of two distinct steps to accomplish this goal, including a photocatalytic Hydrogen Atom Transfer and an ensuing Horner–Wadsworth–Emmons (HWE) reaction. This practical protocol enables the modular and scalable allylation of valuable building blocks and has been applied to structurally complex molecules. The Royal Society of Chemistry 2022-05-31 /pmc/articles/PMC9214841/ /pubmed/35799818 http://dx.doi.org/10.1039/d2sc01581a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Capaldo, Luca
Bonciolini, Stefano
Pulcinella, Antonio
Nuño, Manuel
Noël, Timothy
Modular allylation of C(sp(3))–H bonds by combining decatungstate photocatalysis and HWE olefination in flow
title Modular allylation of C(sp(3))–H bonds by combining decatungstate photocatalysis and HWE olefination in flow
title_full Modular allylation of C(sp(3))–H bonds by combining decatungstate photocatalysis and HWE olefination in flow
title_fullStr Modular allylation of C(sp(3))–H bonds by combining decatungstate photocatalysis and HWE olefination in flow
title_full_unstemmed Modular allylation of C(sp(3))–H bonds by combining decatungstate photocatalysis and HWE olefination in flow
title_short Modular allylation of C(sp(3))–H bonds by combining decatungstate photocatalysis and HWE olefination in flow
title_sort modular allylation of c(sp(3))–h bonds by combining decatungstate photocatalysis and hwe olefination in flow
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214841/
https://www.ncbi.nlm.nih.gov/pubmed/35799818
http://dx.doi.org/10.1039/d2sc01581a
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