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Synthesis of Azidodifluoromethyl Phenyl Sulfone and Its Use as a Synthetic Equivalent of the Azidodifluoromethyl Anion
[Image: see text] Azidodifluoromethyl phenyl sulfone, a new stable fluorinated azide, was synthesized on a multi-gram scale from difluoromethyl phenyl sulfone. The synthetic utility of the title azide in the preparation of N-difluoro(phenylsulfonyl)methyl-1,2,3-triazoles was demonstrated on examples...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242755/ https://www.ncbi.nlm.nih.gov/pubmed/37198902 http://dx.doi.org/10.1021/acs.joc.3c00256 |
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author | Ziabko, Mykyta Klepetářová, Blanka Beier, Petr |
author_facet | Ziabko, Mykyta Klepetářová, Blanka Beier, Petr |
author_sort | Ziabko, Mykyta |
collection | PubMed |
description | [Image: see text] Azidodifluoromethyl phenyl sulfone, a new stable fluorinated azide, was synthesized on a multi-gram scale from difluoromethyl phenyl sulfone. The synthetic utility of the title azide in the preparation of N-difluoro(phenylsulfonyl)methyl-1,2,3-triazoles was demonstrated on examples of azide–alkyne cycloaddition reactions. Subsequent reductive desulfonylation/silylation afforded N-difluoro(trimethylsilyl)methyl-1,2,3-triazoles, and rhodium(II)-catalyzed transannulation with nitriles provided N-difluoro(phenylsulfonyl)methyl-substituted imidazoles. The title azide thus represents a synthetic equivalent of the azidodifluoromethyl anion. |
format | Online Article Text |
id | pubmed-10242755 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-102427552023-06-07 Synthesis of Azidodifluoromethyl Phenyl Sulfone and Its Use as a Synthetic Equivalent of the Azidodifluoromethyl Anion Ziabko, Mykyta Klepetářová, Blanka Beier, Petr J Org Chem [Image: see text] Azidodifluoromethyl phenyl sulfone, a new stable fluorinated azide, was synthesized on a multi-gram scale from difluoromethyl phenyl sulfone. The synthetic utility of the title azide in the preparation of N-difluoro(phenylsulfonyl)methyl-1,2,3-triazoles was demonstrated on examples of azide–alkyne cycloaddition reactions. Subsequent reductive desulfonylation/silylation afforded N-difluoro(trimethylsilyl)methyl-1,2,3-triazoles, and rhodium(II)-catalyzed transannulation with nitriles provided N-difluoro(phenylsulfonyl)methyl-substituted imidazoles. The title azide thus represents a synthetic equivalent of the azidodifluoromethyl anion. American Chemical Society 2023-05-18 /pmc/articles/PMC10242755/ /pubmed/37198902 http://dx.doi.org/10.1021/acs.joc.3c00256 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/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 | Ziabko, Mykyta Klepetářová, Blanka Beier, Petr Synthesis of Azidodifluoromethyl Phenyl Sulfone and Its Use as a Synthetic Equivalent of the Azidodifluoromethyl Anion |
title | Synthesis of Azidodifluoromethyl
Phenyl Sulfone and
Its Use as a Synthetic Equivalent of the Azidodifluoromethyl Anion |
title_full | Synthesis of Azidodifluoromethyl
Phenyl Sulfone and
Its Use as a Synthetic Equivalent of the Azidodifluoromethyl Anion |
title_fullStr | Synthesis of Azidodifluoromethyl
Phenyl Sulfone and
Its Use as a Synthetic Equivalent of the Azidodifluoromethyl Anion |
title_full_unstemmed | Synthesis of Azidodifluoromethyl
Phenyl Sulfone and
Its Use as a Synthetic Equivalent of the Azidodifluoromethyl Anion |
title_short | Synthesis of Azidodifluoromethyl
Phenyl Sulfone and
Its Use as a Synthetic Equivalent of the Azidodifluoromethyl Anion |
title_sort | synthesis of azidodifluoromethyl
phenyl sulfone and
its use as a synthetic equivalent of the azidodifluoromethyl anion |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10242755/ https://www.ncbi.nlm.nih.gov/pubmed/37198902 http://dx.doi.org/10.1021/acs.joc.3c00256 |
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