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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...

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Autores principales: Kazemnejadi, M., Shakeri, A., Nikookar, M., Shademani, R., Mohammadi, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2018
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.
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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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