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The chemistry of isoindole natural products

This review highlights the chemical and biological aspects of natural products containing an oxidized or reduced isoindole skeleton. This motif is found in its intact or modified form in indolocarbazoles, macrocyclic polyketides (cytochalasan alkaloids), the aporhoeadane alkaloids, meroterpenoids fr...

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Detalles Bibliográficos
Autores principales: Speck, Klaus, Magauer, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817534/
https://www.ncbi.nlm.nih.gov/pubmed/24204418
http://dx.doi.org/10.3762/bjoc.9.243
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author Speck, Klaus
Magauer, Thomas
author_facet Speck, Klaus
Magauer, Thomas
author_sort Speck, Klaus
collection PubMed
description This review highlights the chemical and biological aspects of natural products containing an oxidized or reduced isoindole skeleton. This motif is found in its intact or modified form in indolocarbazoles, macrocyclic polyketides (cytochalasan alkaloids), the aporhoeadane alkaloids, meroterpenoids from Stachybotrys species and anthraquinone-type alkaloids. Concerning their biological activity, molecular structure and synthesis, we have limited this review to the most inspiring examples. Within different congeners, we have selected a few members and discussed the synthetic routes in more detail. The putative biosynthetic pathways of the presented isoindole alkaloids are described as well.
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spelling pubmed-38175342013-11-07 The chemistry of isoindole natural products Speck, Klaus Magauer, Thomas Beilstein J Org Chem Review This review highlights the chemical and biological aspects of natural products containing an oxidized or reduced isoindole skeleton. This motif is found in its intact or modified form in indolocarbazoles, macrocyclic polyketides (cytochalasan alkaloids), the aporhoeadane alkaloids, meroterpenoids from Stachybotrys species and anthraquinone-type alkaloids. Concerning their biological activity, molecular structure and synthesis, we have limited this review to the most inspiring examples. Within different congeners, we have selected a few members and discussed the synthetic routes in more detail. The putative biosynthetic pathways of the presented isoindole alkaloids are described as well. Beilstein-Institut 2013-10-10 /pmc/articles/PMC3817534/ /pubmed/24204418 http://dx.doi.org/10.3762/bjoc.9.243 Text en Copyright © 2013, Speck and Magauer 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 Review
Speck, Klaus
Magauer, Thomas
The chemistry of isoindole natural products
title The chemistry of isoindole natural products
title_full The chemistry of isoindole natural products
title_fullStr The chemistry of isoindole natural products
title_full_unstemmed The chemistry of isoindole natural products
title_short The chemistry of isoindole natural products
title_sort chemistry of isoindole natural products
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817534/
https://www.ncbi.nlm.nih.gov/pubmed/24204418
http://dx.doi.org/10.3762/bjoc.9.243
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