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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...

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Detalles Bibliográficos
Autores principales: Włodarczyk, Katarzyna, Borowski, Piotr, Stankevič, Marek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2020
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.
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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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