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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...

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Detalles Bibliográficos
Autores principales: Barta, Petra, Fülöp, Ferenc, Szatmári, István
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
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.
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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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