Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Yu, Ning, Lv, Jing-Fang, He, Shi-Mei, Cui, Yanyan, Wei, Ye, Jiang, Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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
_version_ 1784848205737885696
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
work_keys_str_mv AT yuning ureasynthesisfromisocyanidesandobenzoylhydroxylaminescatalyzedbyacoppersalt
AT lvjingfang ureasynthesisfromisocyanidesandobenzoylhydroxylaminescatalyzedbyacoppersalt
AT heshimei ureasynthesisfromisocyanidesandobenzoylhydroxylaminescatalyzedbyacoppersalt
AT cuiyanyan ureasynthesisfromisocyanidesandobenzoylhydroxylaminescatalyzedbyacoppersalt
AT weiye ureasynthesisfromisocyanidesandobenzoylhydroxylaminescatalyzedbyacoppersalt
AT jiangkun ureasynthesisfromisocyanidesandobenzoylhydroxylaminescatalyzedbyacoppersalt