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Straightforward Access to Thiocyanates via Dealkylative Cyanation of Sulfoxides
[Image: see text] Thiocyanates, versatile building blocks in organic synthesis, are shown to be easily accessible via an interrupted Pummerer reaction of sulfoxides. This facile dealkylative functionalization proceeds under mild conditions through electrophilic activation of the sulfoxide partner. T...
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/PMC8022320/ https://www.ncbi.nlm.nih.gov/pubmed/33724046 http://dx.doi.org/10.1021/acs.orglett.1c00460 |
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author | Todorović, Uroš Klose, Immo Maulide, Nuno |
author_facet | Todorović, Uroš Klose, Immo Maulide, Nuno |
author_sort | Todorović, Uroš |
collection | PubMed |
description | [Image: see text] Thiocyanates, versatile building blocks in organic synthesis, are shown to be easily accessible via an interrupted Pummerer reaction of sulfoxides. This facile dealkylative functionalization proceeds under mild conditions through electrophilic activation of the sulfoxide partner. The resulting thiocyanate itself can serve as a handle for diversification in a straightforward one-pot procedure. |
format | Online Article Text |
id | pubmed-8022320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-80223202021-04-06 Straightforward Access to Thiocyanates via Dealkylative Cyanation of Sulfoxides Todorović, Uroš Klose, Immo Maulide, Nuno Org Lett [Image: see text] Thiocyanates, versatile building blocks in organic synthesis, are shown to be easily accessible via an interrupted Pummerer reaction of sulfoxides. This facile dealkylative functionalization proceeds under mild conditions through electrophilic activation of the sulfoxide partner. The resulting thiocyanate itself can serve as a handle for diversification in a straightforward one-pot procedure. American Chemical Society 2021-03-16 2021-04-02 /pmc/articles/PMC8022320/ /pubmed/33724046 http://dx.doi.org/10.1021/acs.orglett.1c00460 Text en © 2021 The Authors. Published by American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Todorović, Uroš Klose, Immo Maulide, Nuno Straightforward Access to Thiocyanates via Dealkylative Cyanation of Sulfoxides |
title | Straightforward Access to Thiocyanates via Dealkylative
Cyanation of Sulfoxides |
title_full | Straightforward Access to Thiocyanates via Dealkylative
Cyanation of Sulfoxides |
title_fullStr | Straightforward Access to Thiocyanates via Dealkylative
Cyanation of Sulfoxides |
title_full_unstemmed | Straightforward Access to Thiocyanates via Dealkylative
Cyanation of Sulfoxides |
title_short | Straightforward Access to Thiocyanates via Dealkylative
Cyanation of Sulfoxides |
title_sort | straightforward access to thiocyanates via dealkylative
cyanation of sulfoxides |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022320/ https://www.ncbi.nlm.nih.gov/pubmed/33724046 http://dx.doi.org/10.1021/acs.orglett.1c00460 |
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