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3β-Acetoxy-lup-20(29)-en-28-yl 1H-1,2,4-triazole-1-carboxylate
The title triterpene, C(35)H(53)N(3)O(4), is a C-28 carbamate derivative of 3β-acetoxybetulin prepared in a one-step reaction from the commercially available 1,1′-carbonyl-di(1,2,4-triazole) (CDT), crystallized from acetone/n-hexane. All rings are trans fused. The carbamate and acetate substituent...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009070/ https://www.ncbi.nlm.nih.gov/pubmed/21589195 http://dx.doi.org/10.1107/S1600536810043515 |
Sumario: | The title triterpene, C(35)H(53)N(3)O(4), is a C-28 carbamate derivative of 3β-acetoxybetulin prepared in a one-step reaction from the commercially available 1,1′-carbonyl-di(1,2,4-triazole) (CDT), crystallized from acetone/n-hexane. All rings are trans fused. The carbamate and acetate substituents are in axial and equatorial positions, respectively. A quantum chemical ab initio Roothaan Hartree–Fock calculation of the equilibrium geometry of the isolated molecule gives values for bond lengths and valency angles in close agreement with experimental values. The calculation also reproduces the observed molecular conformation, with puckering parameters that agree well with those determined from the crystallographic study. |
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