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Urea Synthesis from Isocyanides and O-Benzoyl Hydroxylamines Catalyzed by a Copper Salt
In the presence of CuOAc, a series of unsymmetric ureas can be generated in moderate to good yields under mild reaction conditions (10 mol% of CuOAc, 2 equiv t-BuONa or PhONa, 30 °C), using aryl isocyanides and O-benzoyl hydroxylamines as the readily accessible starting materials. The reactions migh...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740992/ https://www.ncbi.nlm.nih.gov/pubmed/36500315 http://dx.doi.org/10.3390/molecules27238219 |
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author | Yu, Ning Lv, Jing-Fang He, Shi-Mei Cui, Yanyan Wei, Ye Jiang, Kun |
author_facet | Yu, Ning Lv, Jing-Fang He, Shi-Mei Cui, Yanyan Wei, Ye Jiang, Kun |
author_sort | Yu, Ning |
collection | PubMed |
description | In the presence of CuOAc, a series of unsymmetric ureas can be generated in moderate to good yields under mild reaction conditions (10 mol% of CuOAc, 2 equiv t-BuONa or PhONa, 30 °C), using aryl isocyanides and O-benzoyl hydroxylamines as the readily accessible starting materials. The reactions might undergo a cascade process involving isocyanide insertion into the N-O bond and Mumm-type rearrangement. This work represents a rare example of isocyanide insertion into N-O bonds, which would extend isocyanide insertion chemistry. |
format | Online Article Text |
id | pubmed-9740992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97409922022-12-11 Urea Synthesis from Isocyanides and O-Benzoyl Hydroxylamines Catalyzed by a Copper Salt Yu, Ning Lv, Jing-Fang He, Shi-Mei Cui, Yanyan Wei, Ye Jiang, Kun Molecules Article In the presence of CuOAc, a series of unsymmetric ureas can be generated in moderate to good yields under mild reaction conditions (10 mol% of CuOAc, 2 equiv t-BuONa or PhONa, 30 °C), using aryl isocyanides and O-benzoyl hydroxylamines as the readily accessible starting materials. The reactions might undergo a cascade process involving isocyanide insertion into the N-O bond and Mumm-type rearrangement. This work represents a rare example of isocyanide insertion into N-O bonds, which would extend isocyanide insertion chemistry. MDPI 2022-11-25 /pmc/articles/PMC9740992/ /pubmed/36500315 http://dx.doi.org/10.3390/molecules27238219 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yu, Ning Lv, Jing-Fang He, Shi-Mei Cui, Yanyan Wei, Ye Jiang, Kun Urea Synthesis from Isocyanides and O-Benzoyl Hydroxylamines Catalyzed by a Copper Salt |
title | Urea Synthesis from Isocyanides and O-Benzoyl Hydroxylamines Catalyzed by a Copper Salt |
title_full | Urea Synthesis from Isocyanides and O-Benzoyl Hydroxylamines Catalyzed by a Copper Salt |
title_fullStr | Urea Synthesis from Isocyanides and O-Benzoyl Hydroxylamines Catalyzed by a Copper Salt |
title_full_unstemmed | Urea Synthesis from Isocyanides and O-Benzoyl Hydroxylamines Catalyzed by a Copper Salt |
title_short | Urea Synthesis from Isocyanides and O-Benzoyl Hydroxylamines Catalyzed by a Copper Salt |
title_sort | urea synthesis from isocyanides and o-benzoyl hydroxylamines catalyzed by a copper salt |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740992/ https://www.ncbi.nlm.nih.gov/pubmed/36500315 http://dx.doi.org/10.3390/molecules27238219 |
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