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Organocatalytic Reduction of Aromatic Nitro Compounds: The Use of Solid-Supported Phenyl(2-quinolyl)methanol

[Image: see text] The reduction of aromatic nitro compounds has been performed employing a catalytic amount of Wang resin-supported phenyl(2-quinolyl)methanol (Wang-PQM) in the presence of an excess of NaBH(4) to regenerate the reactive reducing species at the end of the process. The reduction produ...

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Autores principales: Giomi, Donatella, Ceccarelli, Jacopo, Salvini, Antonella, Pinto, Marika, Brandi, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9535724/
https://www.ncbi.nlm.nih.gov/pubmed/36211086
http://dx.doi.org/10.1021/acsomega.2c04196
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author Giomi, Donatella
Ceccarelli, Jacopo
Salvini, Antonella
Pinto, Marika
Brandi, Alberto
author_facet Giomi, Donatella
Ceccarelli, Jacopo
Salvini, Antonella
Pinto, Marika
Brandi, Alberto
author_sort Giomi, Donatella
collection PubMed
description [Image: see text] The reduction of aromatic nitro compounds has been performed employing a catalytic amount of Wang resin-supported phenyl(2-quinolyl)methanol (Wang-PQM) in the presence of an excess of NaBH(4) to regenerate the reactive reducing species at the end of the process. The reduction products are easily isolated through a simple filtration/extraction protocol, and the catalyst can be efficiently recovered and recycled. The condensation route is generally preferred, and azo- and/or hydrazo-arenes can be easily prepared in high yields.
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spelling pubmed-95357242022-10-07 Organocatalytic Reduction of Aromatic Nitro Compounds: The Use of Solid-Supported Phenyl(2-quinolyl)methanol Giomi, Donatella Ceccarelli, Jacopo Salvini, Antonella Pinto, Marika Brandi, Alberto ACS Omega [Image: see text] The reduction of aromatic nitro compounds has been performed employing a catalytic amount of Wang resin-supported phenyl(2-quinolyl)methanol (Wang-PQM) in the presence of an excess of NaBH(4) to regenerate the reactive reducing species at the end of the process. The reduction products are easily isolated through a simple filtration/extraction protocol, and the catalyst can be efficiently recovered and recycled. The condensation route is generally preferred, and azo- and/or hydrazo-arenes can be easily prepared in high yields. American Chemical Society 2022-09-23 /pmc/articles/PMC9535724/ /pubmed/36211086 http://dx.doi.org/10.1021/acsomega.2c04196 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Giomi, Donatella
Ceccarelli, Jacopo
Salvini, Antonella
Pinto, Marika
Brandi, Alberto
Organocatalytic Reduction of Aromatic Nitro Compounds: The Use of Solid-Supported Phenyl(2-quinolyl)methanol
title Organocatalytic Reduction of Aromatic Nitro Compounds: The Use of Solid-Supported Phenyl(2-quinolyl)methanol
title_full Organocatalytic Reduction of Aromatic Nitro Compounds: The Use of Solid-Supported Phenyl(2-quinolyl)methanol
title_fullStr Organocatalytic Reduction of Aromatic Nitro Compounds: The Use of Solid-Supported Phenyl(2-quinolyl)methanol
title_full_unstemmed Organocatalytic Reduction of Aromatic Nitro Compounds: The Use of Solid-Supported Phenyl(2-quinolyl)methanol
title_short Organocatalytic Reduction of Aromatic Nitro Compounds: The Use of Solid-Supported Phenyl(2-quinolyl)methanol
title_sort organocatalytic reduction of aromatic nitro compounds: the use of solid-supported phenyl(2-quinolyl)methanol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9535724/
https://www.ncbi.nlm.nih.gov/pubmed/36211086
http://dx.doi.org/10.1021/acsomega.2c04196
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