dc.creatorESTEVEZ-HERNANDEZ, O.
dc.creatorCORREA, Rodrigo S.
dc.creatorELLENA, Javier
dc.creatorDUQUE, J.
dc.date.accessioned2012-04-19T15:36:25Z
dc.date.accessioned2018-07-04T14:42:49Z
dc.date.available2012-04-19T15:36:25Z
dc.date.available2018-07-04T14:42:49Z
dc.date.created2012-04-19T15:36:25Z
dc.date.issued2009
dc.identifierACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, v.65, p.O648-U2960, 2009
dc.identifier1600-5368
dc.identifierhttp://producao.usp.br/handle/BDPI/16593
dc.identifier10.1107/S1600536808044085
dc.identifierhttp://dx.doi.org/10.1107/S1600536808044085
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1613415
dc.description.abstractThe 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.languageeng
dc.publisherWILEY-BLACKWELL PUBLISHING, INC
dc.relationActa Crystallographica Section E-structure Reports Online
dc.rightsCopyright WILEY-BLACKWELL PUBLISHING, INC
dc.rightsclosedAccess
dc.titleRedetermination of 1-benzyl-3-furoyl-1-phenylthiourea
dc.typeArtículos de revistas


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