2026-05-12T00:27:16Zhttps://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
García Valverde, María
222
500
Marcaccini, Stefano .
521770f8-b058-4536-94f1-0b16031bf7d6
500
González Ortega, Alfonso .
3eb69046-344a-48bd-bd00-44d54652512c
500
Rodríguez Vidal, Francisco Javier
482
500
Rojo Cámara, Mª Josefa
485
500
Torroba Pérez, Tomás
554
500
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
THUMBNAIL
García-OBC_2013.pdf.jpg
García-OBC_2013.pdf.jpg
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García-OBC_2013.pdf
García-OBC_2013.pdf
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LICENSE
license.txt
license.txt
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https://riubu.ubu.es/bitstream/10259/4878/2/license.txt
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TEXT
García-OBC_2013.pdf.txt
García-OBC_2013.pdf.txt
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10259/4878
oai:riubu.ubu.es:10259/4878
2021-11-10 10:38:19.681
Repositorio Institucional de la Universidad de Burgos
bubrep@ubu.es
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