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Selective and metal-free epoxidation of terminal alkenes by heterogeneous polydioxirane in mild conditions
Polydioxirane (PDOX) was prepared by the treatment of polysalicylaldehyde with Oxone and was found as a selective, highly efficient and heterogeneous reagent for epoxidation of alkenes which can be successfully isolated. This work also introduced a simpler, safer and milder way for epoxidation of al...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society Publishing
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990723/ https://www.ncbi.nlm.nih.gov/pubmed/29892358 http://dx.doi.org/10.1098/rsos.171541 |
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author | Kazemnejadi, M. Shakeri, A. Nikookar, M. Shademani, R. Mohammadi, M. |
author_facet | Kazemnejadi, M. Shakeri, A. Nikookar, M. Shademani, R. Mohammadi, M. |
author_sort | Kazemnejadi, M. |
collection | PubMed |
description | Polydioxirane (PDOX) was prepared by the treatment of polysalicylaldehyde with Oxone and was found as a selective, highly efficient and heterogeneous reagent for epoxidation of alkenes which can be successfully isolated. This work also introduced a simpler, safer and milder way for epoxidation of alkenes with dioxirane groups than before. PDOX can be simply recovered from the reaction mixture by plain filtration and reused for eight runs without significant reactivity loss. |
format | Online Article Text |
id | pubmed-5990723 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-59907232018-06-11 Selective and metal-free epoxidation of terminal alkenes by heterogeneous polydioxirane in mild conditions Kazemnejadi, M. Shakeri, A. Nikookar, M. Shademani, R. Mohammadi, M. R Soc Open Sci Chemistry Polydioxirane (PDOX) was prepared by the treatment of polysalicylaldehyde with Oxone and was found as a selective, highly efficient and heterogeneous reagent for epoxidation of alkenes which can be successfully isolated. This work also introduced a simpler, safer and milder way for epoxidation of alkenes with dioxirane groups than before. PDOX can be simply recovered from the reaction mixture by plain filtration and reused for eight runs without significant reactivity loss. The Royal Society Publishing 2018-05-02 /pmc/articles/PMC5990723/ /pubmed/29892358 http://dx.doi.org/10.1098/rsos.171541 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Chemistry Kazemnejadi, M. Shakeri, A. Nikookar, M. Shademani, R. Mohammadi, M. Selective and metal-free epoxidation of terminal alkenes by heterogeneous polydioxirane in mild conditions |
title | Selective and metal-free epoxidation of terminal alkenes by heterogeneous polydioxirane in mild conditions |
title_full | Selective and metal-free epoxidation of terminal alkenes by heterogeneous polydioxirane in mild conditions |
title_fullStr | Selective and metal-free epoxidation of terminal alkenes by heterogeneous polydioxirane in mild conditions |
title_full_unstemmed | Selective and metal-free epoxidation of terminal alkenes by heterogeneous polydioxirane in mild conditions |
title_short | Selective and metal-free epoxidation of terminal alkenes by heterogeneous polydioxirane in mild conditions |
title_sort | selective and metal-free epoxidation of terminal alkenes by heterogeneous polydioxirane in mild conditions |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990723/ https://www.ncbi.nlm.nih.gov/pubmed/29892358 http://dx.doi.org/10.1098/rsos.171541 |
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