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Synthesis of Marine Polycyclic Polyethers via Endo-Selective Epoxide-Opening Cascades

The proposed biosynthetic pathways to ladder polyethers of polyketide origin and oxasqualenoids of terpenoid origin share a dramatic epoxide-opening cascade as a key step. Polycyclic structures generated in these biosynthetic pathways display biological effects ranging from potentially therapeutic p...

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Detalles Bibliográficos
Autores principales: Vilotijevic, Ivan, Jamison, Timothy F.
Formato: Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2857356/
https://www.ncbi.nlm.nih.gov/pubmed/20411125
http://dx.doi.org/10.3390/md8030763
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author Vilotijevic, Ivan
Jamison, Timothy F.
author_facet Vilotijevic, Ivan
Jamison, Timothy F.
author_sort Vilotijevic, Ivan
collection PubMed
description The proposed biosynthetic pathways to ladder polyethers of polyketide origin and oxasqualenoids of terpenoid origin share a dramatic epoxide-opening cascade as a key step. Polycyclic structures generated in these biosynthetic pathways display biological effects ranging from potentially therapeutic properties to extreme lethality. Much of the structural complexity of ladder polyether and oxasqualenoid natural products can be traced to these hypothesized cascades. In this review we summarize how such epoxide-opening cascade reactions have been used in the synthesis of ladder polyethers and oxasqualenoid natural products.
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spelling pubmed-28573562010-04-21 Synthesis of Marine Polycyclic Polyethers via Endo-Selective Epoxide-Opening Cascades Vilotijevic, Ivan Jamison, Timothy F. Mar Drugs Review The proposed biosynthetic pathways to ladder polyethers of polyketide origin and oxasqualenoids of terpenoid origin share a dramatic epoxide-opening cascade as a key step. Polycyclic structures generated in these biosynthetic pathways display biological effects ranging from potentially therapeutic properties to extreme lethality. Much of the structural complexity of ladder polyether and oxasqualenoid natural products can be traced to these hypothesized cascades. In this review we summarize how such epoxide-opening cascade reactions have been used in the synthesis of ladder polyethers and oxasqualenoid natural products. Molecular Diversity Preservation International 2010-03-19 /pmc/articles/PMC2857356/ /pubmed/20411125 http://dx.doi.org/10.3390/md8030763 Text en © 2010 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Vilotijevic, Ivan
Jamison, Timothy F.
Synthesis of Marine Polycyclic Polyethers via Endo-Selective Epoxide-Opening Cascades
title Synthesis of Marine Polycyclic Polyethers via Endo-Selective Epoxide-Opening Cascades
title_full Synthesis of Marine Polycyclic Polyethers via Endo-Selective Epoxide-Opening Cascades
title_fullStr Synthesis of Marine Polycyclic Polyethers via Endo-Selective Epoxide-Opening Cascades
title_full_unstemmed Synthesis of Marine Polycyclic Polyethers via Endo-Selective Epoxide-Opening Cascades
title_short Synthesis of Marine Polycyclic Polyethers via Endo-Selective Epoxide-Opening Cascades
title_sort synthesis of marine polycyclic polyethers via endo-selective epoxide-opening cascades
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2857356/
https://www.ncbi.nlm.nih.gov/pubmed/20411125
http://dx.doi.org/10.3390/md8030763
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