2026-06-17T18:28:29Zhttps://riubu.ubu.es/oai/request

oai:riubu.ubu.es:10259/48782021-11-10T09:38:19Zcom_10259_3924com_10259_5086com_10259_2604com_10259_4354col_10259_3925col_10259_4355

García Valverde, María Marcaccini, Stefano . González Ortega, Alfonso . Rodríguez Vidal, Francisco Javier Rojo Cámara, Mª Josefa Torroba Pérez, Tomás 2018-08-23T10:50:25Z 2018-08-23T10:50:25Z 2013-02 1477-0520 http://hdl.handle.net/10259/4878 10.1039/C2OB27098F Complementary regioselective synthesis of iminohydantoins from isocyanoacetamides controlled by the substituent on the amide group has been described. 4-Iminohydantoins were the major products when the starting materials were N-alkyl isocyanoamides, whereas 2-iminohydantoins were the major products with N-aryl isocyanoamides. Ministerio de Ciencia e Innovación, Spain (Project CTQ2009-12631- BQU), Junta de Castilla y León, Consejería de Educación y Cultura y Fondo Social Europeo (Projects BU023A09 and GR170). application/pdf eng Royal Society of Chemistry Organic & Biomolecular Chemistry. 2014, V. 11, n. 5, p. 721-725 https://doi.org/10.1039/C2OB27098F info:eu-repo/grantAgreement/MICINN/CTQ2009-12631- BQU info:eu-repo/grantAgreement/JCyL/BU023A09 info:eu-repo/grantAgreement/JCyL/GR170 Química orgánica Chemistry, Organic Complementary regioselectivity in the synthesis of iminohydantoins: remarkable effect of amide substitution on the cyclization info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion info:eu-repo/semantics/openAccess