dc.creator | ESTEVEZ-HERNANDEZ, O. | |
dc.creator | CORREA, Rodrigo S. | |
dc.creator | ELLENA, Javier | |
dc.creator | DUQUE, J. | |
dc.date.accessioned | 2012-04-19T15:36:25Z | |
dc.date.accessioned | 2018-07-04T14:42:49Z | |
dc.date.available | 2012-04-19T15:36:25Z | |
dc.date.available | 2018-07-04T14:42:49Z | |
dc.date.created | 2012-04-19T15:36:25Z | |
dc.date.issued | 2009 | |
dc.identifier | ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, v.65, p.O648-U2960, 2009 | |
dc.identifier | 1600-5368 | |
dc.identifier | http://producao.usp.br/handle/BDPI/16593 | |
dc.identifier | 10.1107/S1600536808044085 | |
dc.identifier | http://dx.doi.org/10.1107/S1600536808044085 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1613415 | |
dc.description.abstract | The title compound, C(19)H(16)N(2)O(2)S, was synthesized from furoyl isothiocyanate and N-benzylaniline in dry acetone and the structure redetermined. The structure [Otazo-Sanchez et al. (2001). J. Chem. Soc. Perkin Trans. 2, pp. 2211-2218] has been re-determined in order to establish the intramolecular and intermolecular interactions. The thiourea group is in the thioamide form. The thiourea group makes a dihedral angle of 29.2 (6)degrees with the furoyl group. In the crystal structure, molecules are linked by intermolecular C-H center dot center dot center dot O interactions, forming one-dimensional chains along the a axis. An intramolecular N-H center dot center dot center dot O hydrogen bond is also present. | |
dc.language | eng | |
dc.publisher | WILEY-BLACKWELL PUBLISHING, INC | |
dc.relation | Acta Crystallographica Section E-structure Reports Online | |
dc.rights | Copyright WILEY-BLACKWELL PUBLISHING, INC | |
dc.rights | closedAccess | |
dc.title | Redetermination of 1-benzyl-3-furoyl-1-phenylthiourea | |
dc.type | Artículos de revistas | |