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Micellar Catalysis as a Tool for C–H Bond Functionalization toward C–C Bond Formation

[Image: see text] Micelles generated upon dissolving surfactants in water can be employed as nanovessels for catalytic transformations, in the so-called micellar catalysis methodology. This review is focused on the use of micellar catalysis in the context of the catalytic functionalization of carbon...

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Autores principales: Borrego, Elena, Caballero, Ana, Pérez, Pedro J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10552653/
https://www.ncbi.nlm.nih.gov/pubmed/37810590
http://dx.doi.org/10.1021/acs.organomet.2c00309
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author Borrego, Elena
Caballero, Ana
Pérez, Pedro J.
author_facet Borrego, Elena
Caballero, Ana
Pérez, Pedro J.
author_sort Borrego, Elena
collection PubMed
description [Image: see text] Micelles generated upon dissolving surfactants in water can be employed as nanovessels for catalytic transformations, in the so-called micellar catalysis methodology. This review is focused on the use of micellar catalysis in the context of the catalytic functionalization of carbon–hydrogen bonds. The micelles accumulate catalyst and reactants in their inner volume in such a high local concentration that kinetics are favored. The consequence is that, in most cases, processes that in conventional organic solvents require high temperatures and long reaction times are achieved in milder conditions when micellar catalysis is employed.
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spelling pubmed-105526532023-10-06 Micellar Catalysis as a Tool for C–H Bond Functionalization toward C–C Bond Formation Borrego, Elena Caballero, Ana Pérez, Pedro J. Organometallics [Image: see text] Micelles generated upon dissolving surfactants in water can be employed as nanovessels for catalytic transformations, in the so-called micellar catalysis methodology. This review is focused on the use of micellar catalysis in the context of the catalytic functionalization of carbon–hydrogen bonds. The micelles accumulate catalyst and reactants in their inner volume in such a high local concentration that kinetics are favored. The consequence is that, in most cases, processes that in conventional organic solvents require high temperatures and long reaction times are achieved in milder conditions when micellar catalysis is employed. American Chemical Society 2022-08-15 /pmc/articles/PMC10552653/ /pubmed/37810590 http://dx.doi.org/10.1021/acs.organomet.2c00309 Text en © 2022 American Chemical Society https://creativecommons.org/licenses/by/4.0/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 Borrego, Elena
Caballero, Ana
Pérez, Pedro J.
Micellar Catalysis as a Tool for C–H Bond Functionalization toward C–C Bond Formation
title Micellar Catalysis as a Tool for C–H Bond Functionalization toward C–C Bond Formation
title_full Micellar Catalysis as a Tool for C–H Bond Functionalization toward C–C Bond Formation
title_fullStr Micellar Catalysis as a Tool for C–H Bond Functionalization toward C–C Bond Formation
title_full_unstemmed Micellar Catalysis as a Tool for C–H Bond Functionalization toward C–C Bond Formation
title_short Micellar Catalysis as a Tool for C–H Bond Functionalization toward C–C Bond Formation
title_sort micellar catalysis as a tool for c–h bond functionalization toward c–c bond formation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10552653/
https://www.ncbi.nlm.nih.gov/pubmed/37810590
http://dx.doi.org/10.1021/acs.organomet.2c00309
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