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[1,3]/[1,4]-Sulfur atom migration in β-hydroxyalkylphosphine sulfides
β-Hydroxyalkylphosphine sulfides undergo [1,3]- or [1,4]-sulfur atom phosphorus-to-carbon migration in the presence of Lewis or Brønsted acids. The direction of sulfur atom migration depends on the type of acid used for the reaction. In the presence of a Brønsted acid, mainly [1,3]-rearrangement is...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Beilstein-Institut
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006489/ https://www.ncbi.nlm.nih.gov/pubmed/32082428 http://dx.doi.org/10.3762/bjoc.16.11 |
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author | Włodarczyk, Katarzyna Borowski, Piotr Stankevič, Marek |
author_facet | Włodarczyk, Katarzyna Borowski, Piotr Stankevič, Marek |
author_sort | Włodarczyk, Katarzyna |
collection | PubMed |
description | β-Hydroxyalkylphosphine sulfides undergo [1,3]- or [1,4]-sulfur atom phosphorus-to-carbon migration in the presence of Lewis or Brønsted acids. The direction of sulfur atom migration depends on the type of acid used for the reaction. In the presence of a Brønsted acid, mainly [1,3]-rearrangement is observed, whereas a Lewis acid catalyzes the [1,4]-sulfur migration. To gain insight into the mechanism of these transformations, the stereochemistry of these rearrangements have been tested, along with the conduction of some control experiments and DFT calculations. |
format | Online Article Text |
id | pubmed-7006489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-70064892020-02-20 [1,3]/[1,4]-Sulfur atom migration in β-hydroxyalkylphosphine sulfides Włodarczyk, Katarzyna Borowski, Piotr Stankevič, Marek Beilstein J Org Chem Full Research Paper β-Hydroxyalkylphosphine sulfides undergo [1,3]- or [1,4]-sulfur atom phosphorus-to-carbon migration in the presence of Lewis or Brønsted acids. The direction of sulfur atom migration depends on the type of acid used for the reaction. In the presence of a Brønsted acid, mainly [1,3]-rearrangement is observed, whereas a Lewis acid catalyzes the [1,4]-sulfur migration. To gain insight into the mechanism of these transformations, the stereochemistry of these rearrangements have been tested, along with the conduction of some control experiments and DFT calculations. Beilstein-Institut 2020-01-21 /pmc/articles/PMC7006489/ /pubmed/32082428 http://dx.doi.org/10.3762/bjoc.16.11 Text en Copyright © 2020, Włodarczyk et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Włodarczyk, Katarzyna Borowski, Piotr Stankevič, Marek [1,3]/[1,4]-Sulfur atom migration in β-hydroxyalkylphosphine sulfides |
title | [1,3]/[1,4]-Sulfur atom migration in β-hydroxyalkylphosphine sulfides |
title_full | [1,3]/[1,4]-Sulfur atom migration in β-hydroxyalkylphosphine sulfides |
title_fullStr | [1,3]/[1,4]-Sulfur atom migration in β-hydroxyalkylphosphine sulfides |
title_full_unstemmed | [1,3]/[1,4]-Sulfur atom migration in β-hydroxyalkylphosphine sulfides |
title_short | [1,3]/[1,4]-Sulfur atom migration in β-hydroxyalkylphosphine sulfides |
title_sort | [1,3]/[1,4]-sulfur atom migration in β-hydroxyalkylphosphine sulfides |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7006489/ https://www.ncbi.nlm.nih.gov/pubmed/32082428 http://dx.doi.org/10.3762/bjoc.16.11 |
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