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Enantiospecific Synthesis of Aniline-Derived Sulfonimidamides
[Image: see text] Reaction of sulfonimidoyl fluorides with anilines and Ca(NTf(2))(2) results in the formation of chiral sulfonimidamides. The reaction proceeds with inversion of the stereocenter at a sulfur atom. Enantiospecificity of the reaction was observed for all studied non-heterocyclic anili...
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/PMC10407922/ https://www.ncbi.nlm.nih.gov/pubmed/37490052 http://dx.doi.org/10.1021/acs.orglett.3c02132 |
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author | Liang, Dong-Dong Lional, Natassa Scheepmaker, Bas Subramaniam, Muthusamy Li, Guanna Miloserdov, Fedor M. Zuilhof, Han |
author_facet | Liang, Dong-Dong Lional, Natassa Scheepmaker, Bas Subramaniam, Muthusamy Li, Guanna Miloserdov, Fedor M. Zuilhof, Han |
author_sort | Liang, Dong-Dong |
collection | PubMed |
description | [Image: see text] Reaction of sulfonimidoyl fluorides with anilines and Ca(NTf(2))(2) results in the formation of chiral sulfonimidamides. The reaction proceeds with inversion of the stereocenter at a sulfur atom. Enantiospecificity of the reaction was observed for all studied non-heterocyclic anilines. Combined experimental and computational mechanistic studies highlight chelate-type coordination of the sulfonimidoyl group to Ca(NTf(2))(2) and the formation of a S(N)2-like transition state, in which leaving F(–) coordinates with the Ca(2+) ion. |
format | Online Article Text |
id | pubmed-10407922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104079222023-08-09 Enantiospecific Synthesis of Aniline-Derived Sulfonimidamides Liang, Dong-Dong Lional, Natassa Scheepmaker, Bas Subramaniam, Muthusamy Li, Guanna Miloserdov, Fedor M. Zuilhof, Han Org Lett [Image: see text] Reaction of sulfonimidoyl fluorides with anilines and Ca(NTf(2))(2) results in the formation of chiral sulfonimidamides. The reaction proceeds with inversion of the stereocenter at a sulfur atom. Enantiospecificity of the reaction was observed for all studied non-heterocyclic anilines. Combined experimental and computational mechanistic studies highlight chelate-type coordination of the sulfonimidoyl group to Ca(NTf(2))(2) and the formation of a S(N)2-like transition state, in which leaving F(–) coordinates with the Ca(2+) ion. American Chemical Society 2023-07-25 /pmc/articles/PMC10407922/ /pubmed/37490052 http://dx.doi.org/10.1021/acs.orglett.3c02132 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 | Liang, Dong-Dong Lional, Natassa Scheepmaker, Bas Subramaniam, Muthusamy Li, Guanna Miloserdov, Fedor M. Zuilhof, Han Enantiospecific Synthesis of Aniline-Derived Sulfonimidamides |
title | Enantiospecific
Synthesis of Aniline-Derived Sulfonimidamides |
title_full | Enantiospecific
Synthesis of Aniline-Derived Sulfonimidamides |
title_fullStr | Enantiospecific
Synthesis of Aniline-Derived Sulfonimidamides |
title_full_unstemmed | Enantiospecific
Synthesis of Aniline-Derived Sulfonimidamides |
title_short | Enantiospecific
Synthesis of Aniline-Derived Sulfonimidamides |
title_sort | enantiospecific
synthesis of aniline-derived sulfonimidamides |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10407922/ https://www.ncbi.nlm.nih.gov/pubmed/37490052 http://dx.doi.org/10.1021/acs.orglett.3c02132 |
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