2024-03-29T11:59:20Zhttps://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
Química orgánica
Chemistry, Organic
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).
2018-08-23T10:50:25Z
2018-08-23T10:50:25Z
2013-02
info:eu-repo/semantics/article
info:eu-repo/semantics/acceptedVersion
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
application/pdf
Royal Society of Chemistry
https://riubu.ubu.es/bitstream/10259/4878/4/Garc%c3%ada-OBC_2013.pdf.jpg
Hispana
TEXT
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RIUBU. Repositorio Institucional de la Universidad de Burgos
http://hdl.handle.net/10259/4878