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Asymmetric Synthesis of S(IV) and S(VI) Stereogenic Centers
[Image: see text] Sulfur can form diverse S(IV) and S(VI) stereogenic centers, of which some have gained significant attention recently due to their increasing use as pharmacophores in drug discovery programs. The preparation of these sulfur stereogenic centers in their enantiopure form has been cha...
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/PMC10052288/ https://www.ncbi.nlm.nih.gov/pubmed/37006767 http://dx.doi.org/10.1021/jacsau.2c00626 |
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author | Zhang, Xin Wang, Fucheng Tan, Choon-Hong |
author_facet | Zhang, Xin Wang, Fucheng Tan, Choon-Hong |
author_sort | Zhang, Xin |
collection | PubMed |
description | [Image: see text] Sulfur can form diverse S(IV) and S(VI) stereogenic centers, of which some have gained significant attention recently due to their increasing use as pharmacophores in drug discovery programs. The preparation of these sulfur stereogenic centers in their enantiopure form has been challenging, and progress made will be discussed in this Perspective. This Perspective summarizes different strategies, with selected works, for asymmetric synthesis of these moieties, including diastereoselective transformations using chiral auxiliaries, enantiospecific transformations of enantiopure sulfur compounds, and catalytic enantioselective synthesis. We will discuss the advantages and limitations of these strategies and will provide our views on how this field will develop. |
format | Online Article Text |
id | pubmed-10052288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-100522882023-03-30 Asymmetric Synthesis of S(IV) and S(VI) Stereogenic Centers Zhang, Xin Wang, Fucheng Tan, Choon-Hong JACS Au [Image: see text] Sulfur can form diverse S(IV) and S(VI) stereogenic centers, of which some have gained significant attention recently due to their increasing use as pharmacophores in drug discovery programs. The preparation of these sulfur stereogenic centers in their enantiopure form has been challenging, and progress made will be discussed in this Perspective. This Perspective summarizes different strategies, with selected works, for asymmetric synthesis of these moieties, including diastereoselective transformations using chiral auxiliaries, enantiospecific transformations of enantiopure sulfur compounds, and catalytic enantioselective synthesis. We will discuss the advantages and limitations of these strategies and will provide our views on how this field will develop. American Chemical Society 2023-02-28 /pmc/articles/PMC10052288/ /pubmed/37006767 http://dx.doi.org/10.1021/jacsau.2c00626 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Zhang, Xin Wang, Fucheng Tan, Choon-Hong Asymmetric Synthesis of S(IV) and S(VI) Stereogenic Centers |
title | Asymmetric Synthesis
of S(IV) and S(VI) Stereogenic
Centers |
title_full | Asymmetric Synthesis
of S(IV) and S(VI) Stereogenic
Centers |
title_fullStr | Asymmetric Synthesis
of S(IV) and S(VI) Stereogenic
Centers |
title_full_unstemmed | Asymmetric Synthesis
of S(IV) and S(VI) Stereogenic
Centers |
title_short | Asymmetric Synthesis
of S(IV) and S(VI) Stereogenic
Centers |
title_sort | asymmetric synthesis
of s(iv) and s(vi) stereogenic
centers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052288/ https://www.ncbi.nlm.nih.gov/pubmed/37006767 http://dx.doi.org/10.1021/jacsau.2c00626 |
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