2026-05-07T08:21:14Zhttps://riubu.ubu.es/oai/requestoai:riubu.ubu.es:10259/49242021-11-10T09:38:25Zcom_10259_3593com_10259_5086com_10259_2604com_10259_3596col_10259_3594col_10259_3597
Rubio Presa, Rubén
493
500
Pedrosa Sáez, María de los Remedios
422
500
Fernández Rodríguez, Manuel A.
174
500
Arnáiz García, Francisco Javier
38
500
Sanz Díez, Roberto
531
500
2018-09-07T10:20:10Z
2018-10-06T02:45:06Z
2017-10
1523-7060
http://hdl.handle.net/10259/4924
10.1021/acs.orglett.7b02792
A novel domino reduction/imine formation/intramolecular cyclization/oxidation for the efficient synthesis of pyrrolo(indolo)[1,2-a]quinoxalines and pyrrolo(indolo)[3,2-c]-quinolines from readily available nitrobenzenes and glycols is reported. The process utilizes the carbonyl byproduct of the initial dioxomolybdenum(VI)-catalyzed reduction of nitroaromatics with glycols as a reagent for the imine generation. This method represents the first sustainable domino reaction for the preparation of biologically relevant heterocycles that internally incorporates the waste formed in the first step to the final product.
Junta de Castilla y León and FEDER
(BU076U16) and Ministerio de Economía
y Competitividad
(MINECO) (CTQ2015-70371-REDT and CTQ2016-75023-
C2-1-P)
application/pdf
eng
American Chemical Society
Organic Letters. 2018, V. 19, n. 19, p. 5470-5473
https://doi.org/10.1021/acs.orglett.7b02792
info:eu-repo/grantAgreement/JCyL/BU076U16
info:eu-repo/grantAgreement/MINECO/CTQ2015-70371-REDT
info:eu-repo/grantAgreement/MINECO/CTQ2016-75023-
C2-1-P
Química orgánica
Chemistry, Organic
Molybdenum-Catalyzed Synthesis of Nitrogenated Polyheterocycles from Nitroarenes and Glycols with Reuse of Waste Reduction By-product
info:eu-repo/semantics/article
info:eu-repo/semantics/acceptedVersion
info:eu-repo/semantics/openAccess
THUMBNAIL
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license.txt
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10259/4924
oai:riubu.ubu.es:10259/4924
2021-11-10 10:38:25.196
Repositorio Institucional de la Universidad de Burgos
bubrep@ubu.es
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