Nonanebis(peroxoic acid): a stable peracid for oxidative bromination of aminoanthracene-9,10-dione

A new protocol for the oxidative bromination of aminoanthracene-9,10-dione, which is highly deactivated towards the electrophilic substitution is investigated. The peracid, nonanebis(peroxoic acid), possesses advantages such as better stability at room temperature, it is easy to prepare and non-shoc...

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Autores principales: Patil, Vilas Venunath, Shankarling, Ganapati Subray
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2014
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077418/
https://www.ncbi.nlm.nih.gov/pubmed/24991241
http://dx.doi.org/10.3762/bjoc.10.90
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author Patil, Vilas Venunath
Shankarling, Ganapati Subray
author_facet Patil, Vilas Venunath
Shankarling, Ganapati Subray
author_sort Patil, Vilas Venunath
collection PubMed
description A new protocol for the oxidative bromination of aminoanthracene-9,10-dione, which is highly deactivated towards the electrophilic substitution is investigated. The peracid, nonanebis(peroxoic acid), possesses advantages such as better stability at room temperature, it is easy to prepare and non-shock sensitiv as compared to the conventional peracids. The present protocol has a broad scope for the bromination of various substituted and unsubstituted aminoanthracene-9,10-diones.
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spelling pubmed-40774182014-07-02 Nonanebis(peroxoic acid): a stable peracid for oxidative bromination of aminoanthracene-9,10-dione Patil, Vilas Venunath Shankarling, Ganapati Subray Beilstein J Org Chem Full Research Paper A new protocol for the oxidative bromination of aminoanthracene-9,10-dione, which is highly deactivated towards the electrophilic substitution is investigated. The peracid, nonanebis(peroxoic acid), possesses advantages such as better stability at room temperature, it is easy to prepare and non-shock sensitiv as compared to the conventional peracids. The present protocol has a broad scope for the bromination of various substituted and unsubstituted aminoanthracene-9,10-diones. Beilstein-Institut 2014-04-24 /pmc/articles/PMC4077418/ /pubmed/24991241 http://dx.doi.org/10.3762/bjoc.10.90 Text en Copyright © 2014, Patil and Shankarling 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
Patil, Vilas Venunath
Shankarling, Ganapati Subray
Nonanebis(peroxoic acid): a stable peracid for oxidative bromination of aminoanthracene-9,10-dione
title Nonanebis(peroxoic acid): a stable peracid for oxidative bromination of aminoanthracene-9,10-dione
title_full Nonanebis(peroxoic acid): a stable peracid for oxidative bromination of aminoanthracene-9,10-dione
title_fullStr Nonanebis(peroxoic acid): a stable peracid for oxidative bromination of aminoanthracene-9,10-dione
title_full_unstemmed Nonanebis(peroxoic acid): a stable peracid for oxidative bromination of aminoanthracene-9,10-dione
title_short Nonanebis(peroxoic acid): a stable peracid for oxidative bromination of aminoanthracene-9,10-dione
title_sort nonanebis(peroxoic acid): a stable peracid for oxidative bromination of aminoanthracene-9,10-dione
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077418/
https://www.ncbi.nlm.nih.gov/pubmed/24991241
http://dx.doi.org/10.3762/bjoc.10.90
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