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A Temperature-Controlled Switch between Fürst–Plattner Rule and Anti-Fürst–Plattner Rule Ring Opening of 2,3-Epoxy-steroids with Various Halide Sources in the Presence of Imidazolium Ionic Liquids
[Image: see text] The ring opening of 2α,3α- and 2β,3β-epoxy-5α-androstan-17-one with halide reagents (AlCl(3), TMSCl, LiCl, and LiBr) was investigated using imidazolium ionic liquids in the dual role of solvent and catalyst. The application of the ionic liquid was shown to result in an increase in...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529608/ https://www.ncbi.nlm.nih.gov/pubmed/34693106 http://dx.doi.org/10.1021/acsomega.1c02470 |
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author | Horváth, Anita Bolla, Kristóf Wachtler, Alexandra Maksó, Lilla Papp, Máté Mahó, Sándor Dubrovay, Zsófia Kóti, János Skoda-Földes, Rita |
author_facet | Horváth, Anita Bolla, Kristóf Wachtler, Alexandra Maksó, Lilla Papp, Máté Mahó, Sándor Dubrovay, Zsófia Kóti, János Skoda-Földes, Rita |
author_sort | Horváth, Anita |
collection | PubMed |
description | [Image: see text] The ring opening of 2α,3α- and 2β,3β-epoxy-5α-androstan-17-one with halide reagents (AlCl(3), TMSCl, LiCl, and LiBr) was investigated using imidazolium ionic liquids in the dual role of solvent and catalyst. The application of the ionic liquid was shown to result in an increase in the amount of the unusual diequatorial halohydrins especially at temperatures above 100 °C. With a careful choice of reaction conditions, the latter derivatives could be produced with 43–96% selectivity depending on the nature of the halide ion. Moreover, the usual diaxial products could also be isolated in 70–85% yields by a proper change in the reaction conditions. The reusability of the ionic liquid was demonstrated in both types of reactions. The structures of the products were proved unequivocally by nuclear magnetic resonance (NMR) measurements including two-dimensional (2D) techniques as well as high-resolution mass spectrometry (HRMS). Based on quantum chemical calculations, the effect of the ionic liquid could be explained by the stabilization of the transition state leading to the diequatorial product. |
format | Online Article Text |
id | pubmed-8529608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-85296082021-10-22 A Temperature-Controlled Switch between Fürst–Plattner Rule and Anti-Fürst–Plattner Rule Ring Opening of 2,3-Epoxy-steroids with Various Halide Sources in the Presence of Imidazolium Ionic Liquids Horváth, Anita Bolla, Kristóf Wachtler, Alexandra Maksó, Lilla Papp, Máté Mahó, Sándor Dubrovay, Zsófia Kóti, János Skoda-Földes, Rita ACS Omega [Image: see text] The ring opening of 2α,3α- and 2β,3β-epoxy-5α-androstan-17-one with halide reagents (AlCl(3), TMSCl, LiCl, and LiBr) was investigated using imidazolium ionic liquids in the dual role of solvent and catalyst. The application of the ionic liquid was shown to result in an increase in the amount of the unusual diequatorial halohydrins especially at temperatures above 100 °C. With a careful choice of reaction conditions, the latter derivatives could be produced with 43–96% selectivity depending on the nature of the halide ion. Moreover, the usual diaxial products could also be isolated in 70–85% yields by a proper change in the reaction conditions. The reusability of the ionic liquid was demonstrated in both types of reactions. The structures of the products were proved unequivocally by nuclear magnetic resonance (NMR) measurements including two-dimensional (2D) techniques as well as high-resolution mass spectrometry (HRMS). Based on quantum chemical calculations, the effect of the ionic liquid could be explained by the stabilization of the transition state leading to the diequatorial product. American Chemical Society 2021-10-05 /pmc/articles/PMC8529608/ /pubmed/34693106 http://dx.doi.org/10.1021/acsomega.1c02470 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Horváth, Anita Bolla, Kristóf Wachtler, Alexandra Maksó, Lilla Papp, Máté Mahó, Sándor Dubrovay, Zsófia Kóti, János Skoda-Földes, Rita A Temperature-Controlled Switch between Fürst–Plattner Rule and Anti-Fürst–Plattner Rule Ring Opening of 2,3-Epoxy-steroids with Various Halide Sources in the Presence of Imidazolium Ionic Liquids |
title | A Temperature-Controlled Switch between Fürst–Plattner
Rule and Anti-Fürst–Plattner Rule Ring Opening of 2,3-Epoxy-steroids
with Various Halide Sources in the Presence of Imidazolium Ionic Liquids |
title_full | A Temperature-Controlled Switch between Fürst–Plattner
Rule and Anti-Fürst–Plattner Rule Ring Opening of 2,3-Epoxy-steroids
with Various Halide Sources in the Presence of Imidazolium Ionic Liquids |
title_fullStr | A Temperature-Controlled Switch between Fürst–Plattner
Rule and Anti-Fürst–Plattner Rule Ring Opening of 2,3-Epoxy-steroids
with Various Halide Sources in the Presence of Imidazolium Ionic Liquids |
title_full_unstemmed | A Temperature-Controlled Switch between Fürst–Plattner
Rule and Anti-Fürst–Plattner Rule Ring Opening of 2,3-Epoxy-steroids
with Various Halide Sources in the Presence of Imidazolium Ionic Liquids |
title_short | A Temperature-Controlled Switch between Fürst–Plattner
Rule and Anti-Fürst–Plattner Rule Ring Opening of 2,3-Epoxy-steroids
with Various Halide Sources in the Presence of Imidazolium Ionic Liquids |
title_sort | temperature-controlled switch between fürst–plattner
rule and anti-fürst–plattner rule ring opening of 2,3-epoxy-steroids
with various halide sources in the presence of imidazolium ionic liquids |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529608/ https://www.ncbi.nlm.nih.gov/pubmed/34693106 http://dx.doi.org/10.1021/acsomega.1c02470 |
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