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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),...
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/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. |
format | Online Article Text |
id | pubmed-9903330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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