2024-03-29T09:23:30Zhttps://riubu.ubu.es/oai/requestoai:riubu.ubu.es:10259/48782021-11-10T09:38:19Zcom_10259_3924com_10259_5086com_10259_2604com_10259_4354col_10259_3925col_10259_4355
Complementary regioselectivity in the synthesis of iminohydantoins: remarkable effect of amide substitution on the cyclization
García Valverde, María
Marcaccini, Stefano .
González Ortega, Alfonso .
Rodríguez Vidal, Francisco Javier
Rojo Cámara, Mª Josefa
Torroba Pérez, Tomás
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.
2018-08-23T10:50:25Z
2018-08-23T10:50:25Z
2013-02
info:eu-repo/semantics/article
1477-0520
http://hdl.handle.net/10259/4878
10.1039/C2OB27098F
eng
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
info:eu-repo/semantics/openAccess
Royal Society of Chemistry