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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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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. |
format | Online Article Text |
id | pubmed-9034239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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