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Metal-Free S-Arylation of Phosphorothioate Diesters and Related Compounds with Diaryliodonium Salts

[Image: see text] We developed a direct metal-free S-arylation of phosphorothioate diesters using diaryliodonium salts. The method allows for the preparation under simple conditions of a broad range of S-aryl phosphorothioates, including complex molecules (e.g., dinucleotide or TADDOL derivatives),...

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Autores principales: Sarkar, Sudeep, Kalek, Marcin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9903330/
https://www.ncbi.nlm.nih.gov/pubmed/36662120
http://dx.doi.org/10.1021/acs.orglett.2c04310
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author Sarkar, Sudeep
Kalek, Marcin
author_facet Sarkar, Sudeep
Kalek, Marcin
author_sort Sarkar, Sudeep
collection PubMed
description [Image: see text] We developed a direct metal-free S-arylation of phosphorothioate diesters using diaryliodonium salts. The method allows for the preparation under simple conditions of a broad range of S-aryl phosphorothioates, including complex molecules (e.g., dinucleotide or TADDOL derivatives), as well as other related organophosphorus compounds arylated at a chalcogen. The reaction proceeds with a full retention of the stereogenic center at the phosphorus atom, opening convenient access to P-chiral products. The mechanism of the reaction was established using DFT calculations.
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spelling pubmed-99033302023-02-08 Metal-Free S-Arylation of Phosphorothioate Diesters and Related Compounds with Diaryliodonium Salts Sarkar, Sudeep Kalek, Marcin Org Lett [Image: see text] We developed a direct metal-free S-arylation of phosphorothioate diesters using diaryliodonium salts. The method allows for the preparation under simple conditions of a broad range of S-aryl phosphorothioates, including complex molecules (e.g., dinucleotide or TADDOL derivatives), as well as other related organophosphorus compounds arylated at a chalcogen. The reaction proceeds with a full retention of the stereogenic center at the phosphorus atom, opening convenient access to P-chiral products. The mechanism of the reaction was established using DFT calculations. American Chemical Society 2023-01-20 /pmc/articles/PMC9903330/ /pubmed/36662120 http://dx.doi.org/10.1021/acs.orglett.2c04310 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 Sarkar, Sudeep
Kalek, Marcin
Metal-Free S-Arylation of Phosphorothioate Diesters and Related Compounds with Diaryliodonium Salts
title Metal-Free S-Arylation of Phosphorothioate Diesters and Related Compounds with Diaryliodonium Salts
title_full Metal-Free S-Arylation of Phosphorothioate Diesters and Related Compounds with Diaryliodonium Salts
title_fullStr Metal-Free S-Arylation of Phosphorothioate Diesters and Related Compounds with Diaryliodonium Salts
title_full_unstemmed Metal-Free S-Arylation of Phosphorothioate Diesters and Related Compounds with Diaryliodonium Salts
title_short Metal-Free S-Arylation of Phosphorothioate Diesters and Related Compounds with Diaryliodonium Salts
title_sort metal-free s-arylation of phosphorothioate diesters and related compounds with diaryliodonium salts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9903330/
https://www.ncbi.nlm.nih.gov/pubmed/36662120
http://dx.doi.org/10.1021/acs.orglett.2c04310
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