A Personal Account on Industrial Collaborations in the Field of C–H Activation

In recent years, transition-metal-catalyzed C–H functionalization has emerged as a potentially greener alternative to classic cross-couplings and as a powerful tool to access complex functional molecules with improved step-economy. This short account relates our experience of industrial collaboratio...

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Autor principal: Olivier Baudoin
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Publicado: Swiss Chemical Society 2021
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Acceso en línea:https://doaj.org/article/87e964336f1247f38c398c33d2bfd7b6
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spelling oai:doaj.org-article:87e964336f1247f38c398c33d2bfd7b62021-11-26T10:14:11ZA Personal Account on Industrial Collaborations in the Field of C–H Activation10.2533/chimia.2021.9670009-42932673-2424https://doaj.org/article/87e964336f1247f38c398c33d2bfd7b62021-11-01T00:00:00Zhttps://doaj.org/toc/0009-4293https://doaj.org/toc/2673-2424In recent years, transition-metal-catalyzed C–H functionalization has emerged as a potentially greener alternative to classic cross-couplings and as a powerful tool to access complex functional molecules with improved step-economy. This short account relates our experience of industrial collaborations in C(sp3)–H bond activation, which were key to the development of this topic in our group. The synthesis of the antianginal drug Ivabradine led us to develop a general approach to benzocyclobutenes, which were further employed in peri cyclic reactions. A follow-up study led us to discover a new method to construct arylcyclopropanes via double C–H activation and the coupling of two alkyl groups. Finally, targeting the herbicide Indaziflam contributed to develop C(sp3)–H activation as a powerful tool to access a variety of relevant indane motifs. We hope that these successful stories will help to stimulate further fruitful Industry-Academia collaborations in the field of synthetic chemistry.Olivier BaudoinSwiss Chemical Societyarticlebioactive moleculescatalysisc-h activationpalladiumChemistryQD1-999DEENFRCHIMIA, Vol 75, Iss 11, Pp 967-971 (2021)
institution DOAJ
collection DOAJ
language DE
EN
FR
topic bioactive molecules
catalysis
c-h activation
palladium
Chemistry
QD1-999
spellingShingle bioactive molecules
catalysis
c-h activation
palladium
Chemistry
QD1-999
Olivier Baudoin
A Personal Account on Industrial Collaborations in the Field of C–H Activation
description In recent years, transition-metal-catalyzed C–H functionalization has emerged as a potentially greener alternative to classic cross-couplings and as a powerful tool to access complex functional molecules with improved step-economy. This short account relates our experience of industrial collaborations in C(sp3)–H bond activation, which were key to the development of this topic in our group. The synthesis of the antianginal drug Ivabradine led us to develop a general approach to benzocyclobutenes, which were further employed in peri cyclic reactions. A follow-up study led us to discover a new method to construct arylcyclopropanes via double C–H activation and the coupling of two alkyl groups. Finally, targeting the herbicide Indaziflam contributed to develop C(sp3)–H activation as a powerful tool to access a variety of relevant indane motifs. We hope that these successful stories will help to stimulate further fruitful Industry-Academia collaborations in the field of synthetic chemistry.
format article
author Olivier Baudoin
author_facet Olivier Baudoin
author_sort Olivier Baudoin
title A Personal Account on Industrial Collaborations in the Field of C–H Activation
title_short A Personal Account on Industrial Collaborations in the Field of C–H Activation
title_full A Personal Account on Industrial Collaborations in the Field of C–H Activation
title_fullStr A Personal Account on Industrial Collaborations in the Field of C–H Activation
title_full_unstemmed A Personal Account on Industrial Collaborations in the Field of C–H Activation
title_sort personal account on industrial collaborations in the field of c–h activation
publisher Swiss Chemical Society
publishDate 2021
url https://doaj.org/article/87e964336f1247f38c398c33d2bfd7b6
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