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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...

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Autores principales: Liang, Dong-Dong, Lional, Natassa, Scheepmaker, Bas, Subramaniam, Muthusamy, Li, Guanna, Miloserdov, Fedor M., Zuilhof, Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
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.
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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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