| Texto completo | |
| Autor(es): |
Martins, Lucimara Julio
;
Simoni, Deborah de Alencar
;
Aparicio, Ricardo
;
Coelho, Fernando
Número total de Autores: 4
|
| Tipo de documento: | Artigo Científico |
| Fonte: | ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS; v. 70, p. 9-pg., 2014-12-01. |
| Resumo | |
The title compound, C18H12Br2O6, was synthesized from Morita-Baylis-Hillman adducts. It incorporates the brominated spiro-hexadienone moiety typically exhibited by compounds of this class that exhibit biological activity. Both the brominated cyclohexadienone and the central five-membered rings are nearly planar (r.m.s. deviations of 0.044 and 0.016 angstrom, respectively), being almost perpendicularly oriented [interplanar angle = 89.47 (5)degrees]. With respect to the central five-membered ring, the brominated cyclohexadienone ring, the benzodioxol ring and the carboxylate fragment make C-O-C-C, O-C-C-C and C-C-C-O dihedral angles of -122.11 (8), -27.20 (11) and -8.40 (12)degrees, respectively. An intramolecular C-H center dot center dot center dot O hydrogen bond occurs. In the crystal, molecules are linked by non-classical C-H center dot center dot center dot O and C-H center dot center dot center dot Br hydrogen bonds resulting in a molecular packing in which the brominated rings are in a head-to-head orientation, forming well marked planes parallel to the b axis. (AU) | |
| Processo FAPESP: | 09/51602-5 - Biologia química: novos alvos moleculares naturais e sintéticos contra o câncer, estudos estruturais, avaliação biológica e modo de ação |
| Beneficiário: | Ronaldo Aloise Pilli |
| Modalidade de apoio: | Auxílio à Pesquisa - Temático |
| Processo FAPESP: | 09/18390-4 - Morita-Baylis-Hillman em síntese: diversidade estrutural e avaliação biológica de espirocicloexadienonas |
| Beneficiário: | Lucimara Júlio Martins |
| Modalidade de apoio: | Bolsas no Brasil - Doutorado |