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Synthesis of pyrimido[1,6-a]quinoxalines via intermolecular trapping of thermally generated acyl(quinoxalin-2-yl)ketenes by Schiff bases

Acyl(quinoxalin-2-yl)ketenes generated by thermal decarbonylation of 3-acylpyrrolo[1,2-a]quinoxaline-1,2,4(5H)-triones react regioselectively with Schiff bases under solvent-free conditions to form pyrimido[1,6-a]quinoxaline derivatives in good yields.

Detalles Bibliográficos
Autores principales: Kasatkina, Svetlana O, Stepanova, Ekaterina E, Dmitriev, Maksim V, Mokrushin, Ivan G, Maslivets, Andrey N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071730/
https://www.ncbi.nlm.nih.gov/pubmed/30112078
http://dx.doi.org/10.3762/bjoc.14.147
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author Kasatkina, Svetlana O
Stepanova, Ekaterina E
Dmitriev, Maksim V
Mokrushin, Ivan G
Maslivets, Andrey N
author_facet Kasatkina, Svetlana O
Stepanova, Ekaterina E
Dmitriev, Maksim V
Mokrushin, Ivan G
Maslivets, Andrey N
author_sort Kasatkina, Svetlana O
collection PubMed
description Acyl(quinoxalin-2-yl)ketenes generated by thermal decarbonylation of 3-acylpyrrolo[1,2-a]quinoxaline-1,2,4(5H)-triones react regioselectively with Schiff bases under solvent-free conditions to form pyrimido[1,6-a]quinoxaline derivatives in good yields.
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spelling pubmed-60717302018-08-15 Synthesis of pyrimido[1,6-a]quinoxalines via intermolecular trapping of thermally generated acyl(quinoxalin-2-yl)ketenes by Schiff bases Kasatkina, Svetlana O Stepanova, Ekaterina E Dmitriev, Maksim V Mokrushin, Ivan G Maslivets, Andrey N Beilstein J Org Chem Full Research Paper Acyl(quinoxalin-2-yl)ketenes generated by thermal decarbonylation of 3-acylpyrrolo[1,2-a]quinoxaline-1,2,4(5H)-triones react regioselectively with Schiff bases under solvent-free conditions to form pyrimido[1,6-a]quinoxaline derivatives in good yields. Beilstein-Institut 2018-07-11 /pmc/articles/PMC6071730/ /pubmed/30112078 http://dx.doi.org/10.3762/bjoc.14.147 Text en Copyright © 2018, Kasatkina et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Kasatkina, Svetlana O
Stepanova, Ekaterina E
Dmitriev, Maksim V
Mokrushin, Ivan G
Maslivets, Andrey N
Synthesis of pyrimido[1,6-a]quinoxalines via intermolecular trapping of thermally generated acyl(quinoxalin-2-yl)ketenes by Schiff bases
title Synthesis of pyrimido[1,6-a]quinoxalines via intermolecular trapping of thermally generated acyl(quinoxalin-2-yl)ketenes by Schiff bases
title_full Synthesis of pyrimido[1,6-a]quinoxalines via intermolecular trapping of thermally generated acyl(quinoxalin-2-yl)ketenes by Schiff bases
title_fullStr Synthesis of pyrimido[1,6-a]quinoxalines via intermolecular trapping of thermally generated acyl(quinoxalin-2-yl)ketenes by Schiff bases
title_full_unstemmed Synthesis of pyrimido[1,6-a]quinoxalines via intermolecular trapping of thermally generated acyl(quinoxalin-2-yl)ketenes by Schiff bases
title_short Synthesis of pyrimido[1,6-a]quinoxalines via intermolecular trapping of thermally generated acyl(quinoxalin-2-yl)ketenes by Schiff bases
title_sort synthesis of pyrimido[1,6-a]quinoxalines via intermolecular trapping of thermally generated acyl(quinoxalin-2-yl)ketenes by schiff bases
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071730/
https://www.ncbi.nlm.nih.gov/pubmed/30112078
http://dx.doi.org/10.3762/bjoc.14.147
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