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Crystal structures of rac-2,3-diphenyl-2,3,5,6-tetra­hydro-4H-1,3-thia­zine-1,1,4-trione and N-[(2S,5R)-1,1,4-trioxo-2,3-diphenyl-1,3-thia­zinan-5-yl]acet­amide

The syntheses and crystal structures of two thia­zinone compounds, namely, rac-2,3-diphenyl-2,3,5,6-tetra­hydro-4H-1,3-thia­zine-1,1,4-trione, C(16)H(15)NO(3)S, in its racemic form, and N-[(2S,5R)-1,1,4-trioxo-2,3-diphenyl-1,3-thia­zinan-5-yl]acet­amide, C(18)H(18)N(2)O(4)S, in an enanti­opure form,...

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Detalles Bibliográficos
Autores principales: Yennawar, Hemant P., Lowe, Saige L., Mammen, Matthew M., Verhagen, Connor R., Silverberg, Lee J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9912464/
https://www.ncbi.nlm.nih.gov/pubmed/36793410
http://dx.doi.org/10.1107/S2056989023000695
Descripción
Sumario:The syntheses and crystal structures of two thia­zinone compounds, namely, rac-2,3-diphenyl-2,3,5,6-tetra­hydro-4H-1,3-thia­zine-1,1,4-trione, C(16)H(15)NO(3)S, in its racemic form, and N-[(2S,5R)-1,1,4-trioxo-2,3-diphenyl-1,3-thia­zinan-5-yl]acet­amide, C(18)H(18)N(2)O(4)S, in an enanti­opure form, are reported. The thia­zine rings in the two structures differ in their puckering, as a half-chair in the first and a boat pucker in the second. The extended structures for both compounds have only C—H⋯O-type inter­actions between symmetry-related mol­ecules, and exhibit no π–π stacking inter­actions in spite of each having two phenyl rings.