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    <subfield code="a">Canudo-Barreras, G.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-1732-9155</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Gold-catalyzed 1, 3-Thiazine formation and uncommon tautomer isolation</subfield>
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    <subfield code="c">2022</subfield>
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    <subfield code="a">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. © 2022 American Chemical Society. All rights reserved.</subfield>
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    <subfield code="a">Organic Chemistry</subfield>
    <subfield code="c">2022</subfield>
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    <subfield code="a">Salvador, D.</subfield>
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    <subfield code="a">Herrera, R. P.</subfield>
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    <subfield code="a">Gimeno, M. C.</subfield>
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    <subfield code="b">Dpto. Ciencias de la Tierra</subfield>
    <subfield code="c">Área Paleontología</subfield>
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    <subfield code="g">87, 16 (2022), 10747-10754</subfield>
    <subfield code="p">J. org. chem.</subfield>
    <subfield code="t">Journal of Organic Chemistry</subfield>
    <subfield code="x">0022-3263</subfield>
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