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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...

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Autores principales: Canudo-Barreras, Guillermo, Salvador, Daniel, Herrera, Raquel P., Gimeno, M. Concepción
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
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.
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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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