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Mannich base-connected syntheses mediated by ortho-quinone methides
This article provides an overview about specifically modified Mannich reactions where the process involves an ortho-quinone methide (o-QM) intermediate. The reactions are classified on the basis of the o-QM source followed by the reactant, e.g., the dienophile partner in cycloaddition reactions (C=C...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852458/ https://www.ncbi.nlm.nih.gov/pubmed/29623118 http://dx.doi.org/10.3762/bjoc.14.43 |
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author | Barta, Petra Fülöp, Ferenc Szatmári, István |
author_facet | Barta, Petra Fülöp, Ferenc Szatmári, István |
author_sort | Barta, Petra |
collection | PubMed |
description | This article provides an overview about specifically modified Mannich reactions where the process involves an ortho-quinone methide (o-QM) intermediate. The reactions are classified on the basis of the o-QM source followed by the reactant, e.g., the dienophile partner in cycloaddition reactions (C=C or C=N dienophiles) or by the formation of multicomponent Mannich adducts. Due to the important pharmacological activities of these reactive o-QM intermediates, special attention is paid to the biological activity of these compounds. |
format | Online Article Text |
id | pubmed-5852458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-58524582018-04-05 Mannich base-connected syntheses mediated by ortho-quinone methides Barta, Petra Fülöp, Ferenc Szatmári, István Beilstein J Org Chem Review This article provides an overview about specifically modified Mannich reactions where the process involves an ortho-quinone methide (o-QM) intermediate. The reactions are classified on the basis of the o-QM source followed by the reactant, e.g., the dienophile partner in cycloaddition reactions (C=C or C=N dienophiles) or by the formation of multicomponent Mannich adducts. Due to the important pharmacological activities of these reactive o-QM intermediates, special attention is paid to the biological activity of these compounds. Beilstein-Institut 2018-03-06 /pmc/articles/PMC5852458/ /pubmed/29623118 http://dx.doi.org/10.3762/bjoc.14.43 Text en Copyright © 2018, Barta 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 | Review Barta, Petra Fülöp, Ferenc Szatmári, István Mannich base-connected syntheses mediated by ortho-quinone methides |
title | Mannich base-connected syntheses mediated by ortho-quinone methides |
title_full | Mannich base-connected syntheses mediated by ortho-quinone methides |
title_fullStr | Mannich base-connected syntheses mediated by ortho-quinone methides |
title_full_unstemmed | Mannich base-connected syntheses mediated by ortho-quinone methides |
title_short | Mannich base-connected syntheses mediated by ortho-quinone methides |
title_sort | mannich base-connected syntheses mediated by ortho-quinone methides |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852458/ https://www.ncbi.nlm.nih.gov/pubmed/29623118 http://dx.doi.org/10.3762/bjoc.14.43 |
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