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3β-Hydroxylup-20(29)-en-28-yl 1H-imidazole-1-carboxylate
The title triterpene, C(34)H(52)N(2)O(3), is a C-28 carbamate derivative of betulin prepared in a one-step reaction from the commercially available 1,1′-carbonyldiimidazole (CDI). All rings are fused trans. The X-ray study shows the retention of the configuration of C-28 with respect to the known c...
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/PMC3007052/ https://www.ncbi.nlm.nih.gov/pubmed/21588073 http://dx.doi.org/10.1107/S160053681002489X |
Sumario: | The title triterpene, C(34)H(52)N(2)O(3), is a C-28 carbamate derivative of betulin prepared in a one-step reaction from the commercially available 1,1′-carbonyldiimidazole (CDI). All rings are fused trans. The X-ray study shows the retention of the configuration of C-28 with respect to the known chiral centres of the molecule. In the crystal, the molecules are O—H⋯O hydrogen bonded via the hydroxy group and the carbonyl group of the carbamate function into chains running along the c axis. A quantum-mechanical ab initio Roothaan Hartree–Fock calculation of the equilibrium geometry of the isolated molecule gives values for bond-lengths and valency angles close to the experimental values. The calculations also reproduce the molecular conformation well, with calculated puckering parameters that agree well with the observed values. |
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