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9,10-Dioxa-1,2-diaza-anthracene derivatives from tetrafluoropyridazine
Reaction of tetrafluoropyridazine with catechol gives a tricyclic 9,10-dioxa-1,2-diaza-anthracene system by a sequential nucleophilic aromatic substitution ring annelation process, further extending the use of perfluoroheteroaromatic derivatives for the synthesis of unusual polyfunctional heterocycl...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887278/ https://www.ncbi.nlm.nih.gov/pubmed/20563272 http://dx.doi.org/10.3762/bjoc.6.45 |
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author | Pattison, Graham Sandford, Graham Yufit, Dmitrii S Howard, Judith A K Christopher, John A Miller, David D |
author_facet | Pattison, Graham Sandford, Graham Yufit, Dmitrii S Howard, Judith A K Christopher, John A Miller, David D |
author_sort | Pattison, Graham |
collection | PubMed |
description | Reaction of tetrafluoropyridazine with catechol gives a tricyclic 9,10-dioxa-1,2-diaza-anthracene system by a sequential nucleophilic aromatic substitution ring annelation process, further extending the use of perfluoroheteroaromatic derivatives for the synthesis of unusual polyfunctional heterocyclic architectures. The tricyclic scaffold reacts with amines and sodium ethoxide providing a short series of functional 9,10-dioxa-1,2-diaza-anthracene systems. |
format | Text |
id | pubmed-2887278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-28872782010-06-18 9,10-Dioxa-1,2-diaza-anthracene derivatives from tetrafluoropyridazine Pattison, Graham Sandford, Graham Yufit, Dmitrii S Howard, Judith A K Christopher, John A Miller, David D Beilstein J Org Chem Full Research Paper Reaction of tetrafluoropyridazine with catechol gives a tricyclic 9,10-dioxa-1,2-diaza-anthracene system by a sequential nucleophilic aromatic substitution ring annelation process, further extending the use of perfluoroheteroaromatic derivatives for the synthesis of unusual polyfunctional heterocyclic architectures. The tricyclic scaffold reacts with amines and sodium ethoxide providing a short series of functional 9,10-dioxa-1,2-diaza-anthracene systems. Beilstein-Institut 2010-05-06 /pmc/articles/PMC2887278/ /pubmed/20563272 http://dx.doi.org/10.3762/bjoc.6.45 Text en Copyright © 2010, Pattison et al. https://creativecommons.org/licenses/by/2.0https://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/2.0), 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 Pattison, Graham Sandford, Graham Yufit, Dmitrii S Howard, Judith A K Christopher, John A Miller, David D 9,10-Dioxa-1,2-diaza-anthracene derivatives from tetrafluoropyridazine |
title | 9,10-Dioxa-1,2-diaza-anthracene derivatives from tetrafluoropyridazine |
title_full | 9,10-Dioxa-1,2-diaza-anthracene derivatives from tetrafluoropyridazine |
title_fullStr | 9,10-Dioxa-1,2-diaza-anthracene derivatives from tetrafluoropyridazine |
title_full_unstemmed | 9,10-Dioxa-1,2-diaza-anthracene derivatives from tetrafluoropyridazine |
title_short | 9,10-Dioxa-1,2-diaza-anthracene derivatives from tetrafluoropyridazine |
title_sort | 9,10-dioxa-1,2-diaza-anthracene derivatives from tetrafluoropyridazine |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887278/ https://www.ncbi.nlm.nih.gov/pubmed/20563272 http://dx.doi.org/10.3762/bjoc.6.45 |
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