Taking electrodecarboxylative etherification beyond Hofer–Moest using a radical C–O coupling strategy

Since its discovery, the Hofer-Moest mechanism strongly limits the scope of electrochemical decarboxylative etherification. Here, the authors report the electrochemical conversion of carboxylic acids into alkyl benzotriazole ethers expanding the scope to primary and secondary acids beyond the bounda...

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Autores principales:	Ángel Manu Martínez, Davit Hayrapetyan, Tim van Lingen, Marco Dyga, Lukas J. Gooßen
Formato:	article
Lenguaje:	EN
Publicado:	Nature Portfolio 2020
Materias:	Science Q
Acceso en línea:	https://doaj.org/article/d177271950004c22b046a1091c8f4a54
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spelling	oai:doaj.org-article:d177271950004c22b046a1091c8f4a542021-12-02T15:27:34ZTaking electrodecarboxylative etherification beyond Hofer–Moest using a radical C–O coupling strategy10.1038/s41467-020-18275-12041-1723https://doaj.org/article/d177271950004c22b046a1091c8f4a542020-09-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-18275-1https://doaj.org/toc/2041-1723Since its discovery, the Hofer-Moest mechanism strongly limits the scope of electrochemical decarboxylative etherification. Here, the authors report the electrochemical conversion of carboxylic acids into alkyl benzotriazole ethers expanding the scope to primary and secondary acids beyond the boundaries of Hofer-Moest-type reactions.Ángel Manu MartínezDavit HayrapetyanTim van LingenMarco DygaLukas J. GooßenNature PortfolioarticleScienceQENNature Communications, Vol 11, Iss 1, Pp 1-8 (2020)
institution	DOAJ
collection	DOAJ
language	EN
topic	Science Q
spellingShingle	Science Q Ángel Manu Martínez Davit Hayrapetyan Tim van Lingen Marco Dyga Lukas J. Gooßen Taking electrodecarboxylative etherification beyond Hofer–Moest using a radical C–O coupling strategy
description	Since its discovery, the Hofer-Moest mechanism strongly limits the scope of electrochemical decarboxylative etherification. Here, the authors report the electrochemical conversion of carboxylic acids into alkyl benzotriazole ethers expanding the scope to primary and secondary acids beyond the boundaries of Hofer-Moest-type reactions.
format	article
author	Ángel Manu Martínez Davit Hayrapetyan Tim van Lingen Marco Dyga Lukas J. Gooßen
author_facet	Ángel Manu Martínez Davit Hayrapetyan Tim van Lingen Marco Dyga Lukas J. Gooßen
author_sort	Ángel Manu Martínez
title	Taking electrodecarboxylative etherification beyond Hofer–Moest using a radical C–O coupling strategy
title_short	Taking electrodecarboxylative etherification beyond Hofer–Moest using a radical C–O coupling strategy
title_full	Taking electrodecarboxylative etherification beyond Hofer–Moest using a radical C–O coupling strategy
title_fullStr	Taking electrodecarboxylative etherification beyond Hofer–Moest using a radical C–O coupling strategy
title_full_unstemmed	Taking electrodecarboxylative etherification beyond Hofer–Moest using a radical C–O coupling strategy
title_sort	taking electrodecarboxylative etherification beyond hofer–moest using a radical c–o coupling strategy
publisher	Nature Portfolio
publishDate	2020
url	https://doaj.org/article/d177271950004c22b046a1091c8f4a54
work_keys_str_mv	AT angelmanumartinez takingelectrodecarboxylativeetherificationbeyondhofermoestusingaradicalcocouplingstrategy AT davithayrapetyan takingelectrodecarboxylativeetherificationbeyondhofermoestusingaradicalcocouplingstrategy AT timvanlingen takingelectrodecarboxylativeetherificationbeyondhofermoestusingaradicalcocouplingstrategy AT marcodyga takingelectrodecarboxylativeetherificationbeyondhofermoestusingaradicalcocouplingstrategy AT lukasjgooßen takingelectrodecarboxylativeetherificationbeyondhofermoestusingaradicalcocouplingstrategy
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Taking electrodecarboxylative etherification beyond Hofer–Moest using a radical C–O coupling strategy

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