Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1784802836049035264 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9535724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT giomidonatella organocatalyticreductionofaromaticnitrocompoundstheuseofsolidsupportedphenyl2quinolylmethanol AT ceccarellijacopo organocatalyticreductionofaromaticnitrocompoundstheuseofsolidsupportedphenyl2quinolylmethanol AT salviniantonella organocatalyticreductionofaromaticnitrocompoundstheuseofsolidsupportedphenyl2quinolylmethanol AT pintomarika organocatalyticreductionofaromaticnitrocompoundstheuseofsolidsupportedphenyl2quinolylmethanol AT brandialberto organocatalyticreductionofaromaticnitrocompoundstheuseofsolidsupportedphenyl2quinolylmethanol |