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A practical method for the aziridination of α,β-unsaturated carbonyl compounds with a simple carbamate utilizing sodium hypochlorite pentahydrate

The efficient formation of tert-butyl N-chloro-N-sodio-carbamate by the reaction of simple tert-butyl carbamate with sodium hypochlorite pentahydrate (NaOCl·5H(2)O) would be a practical and green method for the aziridination of α,β-unsaturated carbonyl compounds. The process described herein is tran...

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Detalles Bibliográficos
Autores principales: Umeda, Takehiro, Minakata, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034239/
https://www.ncbi.nlm.nih.gov/pubmed/35480842
http://dx.doi.org/10.1039/d1ra04297a
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author Umeda, Takehiro
Minakata, Satoshi
author_facet Umeda, Takehiro
Minakata, Satoshi
author_sort Umeda, Takehiro
collection PubMed
description The efficient formation of tert-butyl N-chloro-N-sodio-carbamate by the reaction of simple tert-butyl carbamate with sodium hypochlorite pentahydrate (NaOCl·5H(2)O) would be a practical and green method for the aziridination of α,β-unsaturated carbonyl compounds. The process described herein is transition-metal free, all of the materials are commercially available, the byproducts (NaCl and H(2)O) are environmentally benign and the reaction is stereoselective. The resulting aziridines are potential precursors of amino acids.
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spelling pubmed-90342392022-04-26 A practical method for the aziridination of α,β-unsaturated carbonyl compounds with a simple carbamate utilizing sodium hypochlorite pentahydrate Umeda, Takehiro Minakata, Satoshi RSC Adv Chemistry The efficient formation of tert-butyl N-chloro-N-sodio-carbamate by the reaction of simple tert-butyl carbamate with sodium hypochlorite pentahydrate (NaOCl·5H(2)O) would be a practical and green method for the aziridination of α,β-unsaturated carbonyl compounds. The process described herein is transition-metal free, all of the materials are commercially available, the byproducts (NaCl and H(2)O) are environmentally benign and the reaction is stereoselective. The resulting aziridines are potential precursors of amino acids. The Royal Society of Chemistry 2021-06-22 /pmc/articles/PMC9034239/ /pubmed/35480842 http://dx.doi.org/10.1039/d1ra04297a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Umeda, Takehiro
Minakata, Satoshi
A practical method for the aziridination of α,β-unsaturated carbonyl compounds with a simple carbamate utilizing sodium hypochlorite pentahydrate
title A practical method for the aziridination of α,β-unsaturated carbonyl compounds with a simple carbamate utilizing sodium hypochlorite pentahydrate
title_full A practical method for the aziridination of α,β-unsaturated carbonyl compounds with a simple carbamate utilizing sodium hypochlorite pentahydrate
title_fullStr A practical method for the aziridination of α,β-unsaturated carbonyl compounds with a simple carbamate utilizing sodium hypochlorite pentahydrate
title_full_unstemmed A practical method for the aziridination of α,β-unsaturated carbonyl compounds with a simple carbamate utilizing sodium hypochlorite pentahydrate
title_short A practical method for the aziridination of α,β-unsaturated carbonyl compounds with a simple carbamate utilizing sodium hypochlorite pentahydrate
title_sort practical method for the aziridination of α,β-unsaturated carbonyl compounds with a simple carbamate utilizing sodium hypochlorite pentahydrate
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034239/
https://www.ncbi.nlm.nih.gov/pubmed/35480842
http://dx.doi.org/10.1039/d1ra04297a
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