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Gold-Catalyzed 1,3-Thiazine Formation and Uncommon Tautomer Isolation
[Image: see text] This work represents the first example of a gold-catalyzed formation of 1,3-thiazine/1,3-thiazinane by means of a catalytic approach and further uncommon isolation of the two tautomers. The developed protocol gives rise to a broad scope of 1,3-thiazine derivatives with excellent yi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9400392/ https://www.ncbi.nlm.nih.gov/pubmed/35944547 http://dx.doi.org/10.1021/acs.joc.2c00947 |
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author | Canudo-Barreras, Guillermo Salvador, Daniel Herrera, Raquel P. Gimeno, M. Concepción |
author_facet | Canudo-Barreras, Guillermo Salvador, Daniel Herrera, Raquel P. Gimeno, M. Concepción |
author_sort | Canudo-Barreras, Guillermo |
collection | PubMed |
description | [Image: see text] This work represents the first example of a gold-catalyzed formation of 1,3-thiazine/1,3-thiazinane by means of a catalytic approach and further uncommon isolation of the two tautomers. The developed protocol gives rise to a broad scope of 1,3-thiazine derivatives with excellent yields in short reaction times. Interestingly, different isomers could be obtained depending on the state of the compound, and in the crystal state the 1,3-thiazinane isomer is obtained, while in solution the 1,3-thiazine is the unique isomer. This work represents an interesting approach for the synthesis of potential biologically relevant molecules and a crucial precedent in tautomerism isolation and characterization. |
format | Online Article Text |
id | pubmed-9400392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-94003922022-08-25 Gold-Catalyzed 1,3-Thiazine Formation and Uncommon Tautomer Isolation Canudo-Barreras, Guillermo Salvador, Daniel Herrera, Raquel P. Gimeno, M. Concepción J Org Chem [Image: see text] This work represents the first example of a gold-catalyzed formation of 1,3-thiazine/1,3-thiazinane by means of a catalytic approach and further uncommon isolation of the two tautomers. The developed protocol gives rise to a broad scope of 1,3-thiazine derivatives with excellent yields in short reaction times. Interestingly, different isomers could be obtained depending on the state of the compound, and in the crystal state the 1,3-thiazinane isomer is obtained, while in solution the 1,3-thiazine is the unique isomer. This work represents an interesting approach for the synthesis of potential biologically relevant molecules and a crucial precedent in tautomerism isolation and characterization. American Chemical Society 2022-08-09 2022-08-19 /pmc/articles/PMC9400392/ /pubmed/35944547 http://dx.doi.org/10.1021/acs.joc.2c00947 Text en © 2022 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 | Canudo-Barreras, Guillermo Salvador, Daniel Herrera, Raquel P. Gimeno, M. Concepción Gold-Catalyzed 1,3-Thiazine Formation and Uncommon Tautomer Isolation |
title | Gold-Catalyzed 1,3-Thiazine
Formation and Uncommon
Tautomer Isolation |
title_full | Gold-Catalyzed 1,3-Thiazine
Formation and Uncommon
Tautomer Isolation |
title_fullStr | Gold-Catalyzed 1,3-Thiazine
Formation and Uncommon
Tautomer Isolation |
title_full_unstemmed | Gold-Catalyzed 1,3-Thiazine
Formation and Uncommon
Tautomer Isolation |
title_short | Gold-Catalyzed 1,3-Thiazine
Formation and Uncommon
Tautomer Isolation |
title_sort | gold-catalyzed 1,3-thiazine
formation and uncommon
tautomer isolation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9400392/ https://www.ncbi.nlm.nih.gov/pubmed/35944547 http://dx.doi.org/10.1021/acs.joc.2c00947 |
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