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Asymmetric Amination of meso-Epoxide with Vegetable Powder as a Low-Toxicity Catalyst
This paper describes the scope and limitation of substrates subjected to asymmetric amination with epoxides catalyzed by a soluble soybean polysaccharide (Soyafibe S-DN), which we recently discovered from the reaction of 1,2-epoxycyclohexane with cyclopropylamine. Various meso-epoxides reacted with...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397229/ https://www.ncbi.nlm.nih.gov/pubmed/32668749 http://dx.doi.org/10.3390/molecules25143197 |
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author | Takeuchi, Yuki Asano, Tatsuhiro Tsuzaki, Kazuya Wada, Koichi Kurata, Hiroyuki |
author_facet | Takeuchi, Yuki Asano, Tatsuhiro Tsuzaki, Kazuya Wada, Koichi Kurata, Hiroyuki |
author_sort | Takeuchi, Yuki |
collection | PubMed |
description | This paper describes the scope and limitation of substrates subjected to asymmetric amination with epoxides catalyzed by a soluble soybean polysaccharide (Soyafibe S-DN), which we recently discovered from the reaction of 1,2-epoxycyclohexane with cyclopropylamine. Various meso-epoxides reacted with various amines afforded the corresponding products with good enantiomeric selectivity. Since it was found that pectin was found to have a catalytic ability after screening commercially available polysaccharides, we studied 33 different vegetable powders having pectic substances, and we found that many vegetable powders showed catalytic ability. These results should guide in using vegetable components as low-toxic catalysts for the production of pharmaceuticals. |
format | Online Article Text |
id | pubmed-7397229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73972292020-08-16 Asymmetric Amination of meso-Epoxide with Vegetable Powder as a Low-Toxicity Catalyst Takeuchi, Yuki Asano, Tatsuhiro Tsuzaki, Kazuya Wada, Koichi Kurata, Hiroyuki Molecules Article This paper describes the scope and limitation of substrates subjected to asymmetric amination with epoxides catalyzed by a soluble soybean polysaccharide (Soyafibe S-DN), which we recently discovered from the reaction of 1,2-epoxycyclohexane with cyclopropylamine. Various meso-epoxides reacted with various amines afforded the corresponding products with good enantiomeric selectivity. Since it was found that pectin was found to have a catalytic ability after screening commercially available polysaccharides, we studied 33 different vegetable powders having pectic substances, and we found that many vegetable powders showed catalytic ability. These results should guide in using vegetable components as low-toxic catalysts for the production of pharmaceuticals. MDPI 2020-07-13 /pmc/articles/PMC7397229/ /pubmed/32668749 http://dx.doi.org/10.3390/molecules25143197 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Takeuchi, Yuki Asano, Tatsuhiro Tsuzaki, Kazuya Wada, Koichi Kurata, Hiroyuki Asymmetric Amination of meso-Epoxide with Vegetable Powder as a Low-Toxicity Catalyst |
title | Asymmetric Amination of meso-Epoxide with Vegetable Powder as a Low-Toxicity Catalyst |
title_full | Asymmetric Amination of meso-Epoxide with Vegetable Powder as a Low-Toxicity Catalyst |
title_fullStr | Asymmetric Amination of meso-Epoxide with Vegetable Powder as a Low-Toxicity Catalyst |
title_full_unstemmed | Asymmetric Amination of meso-Epoxide with Vegetable Powder as a Low-Toxicity Catalyst |
title_short | Asymmetric Amination of meso-Epoxide with Vegetable Powder as a Low-Toxicity Catalyst |
title_sort | asymmetric amination of meso-epoxide with vegetable powder as a low-toxicity catalyst |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7397229/ https://www.ncbi.nlm.nih.gov/pubmed/32668749 http://dx.doi.org/10.3390/molecules25143197 |
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