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Self-Assembly of Disorazole C(1) through a One-Pot Alkyne Metathesis Homodimerization Strategy**

Alkyne metathesis is increasingly explored as a reliable method to close macrocyclic rings, but there are no prior examples of an alkyne-metathesis-based homodimerization approach to natural products. In this approach to the cytotoxic C(2)-symmetric marine-derived bis(lactone) disorazole C(1), a hig...

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Autores principales: Ralston, Kevin J, Ramstadius, H Clinton, Brewster, Richard C, Niblock, Helen S, Hulme, Alison N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517162/
https://www.ncbi.nlm.nih.gov/pubmed/25926364
http://dx.doi.org/10.1002/anie.201501922
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author Ralston, Kevin J
Ramstadius, H Clinton
Brewster, Richard C
Niblock, Helen S
Hulme, Alison N
author_facet Ralston, Kevin J
Ramstadius, H Clinton
Brewster, Richard C
Niblock, Helen S
Hulme, Alison N
author_sort Ralston, Kevin J
collection PubMed
description Alkyne metathesis is increasingly explored as a reliable method to close macrocyclic rings, but there are no prior examples of an alkyne-metathesis-based homodimerization approach to natural products. In this approach to the cytotoxic C(2)-symmetric marine-derived bis(lactone) disorazole C(1), a highly convergent, modular strategy is employed featuring cyclization through an ambitious one-pot alkyne cross-metathesis/ring-closing metathesis self-assembly process.
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spelling pubmed-45171622015-08-04 Self-Assembly of Disorazole C(1) through a One-Pot Alkyne Metathesis Homodimerization Strategy** Ralston, Kevin J Ramstadius, H Clinton Brewster, Richard C Niblock, Helen S Hulme, Alison N Angew Chem Int Ed Engl Communications Alkyne metathesis is increasingly explored as a reliable method to close macrocyclic rings, but there are no prior examples of an alkyne-metathesis-based homodimerization approach to natural products. In this approach to the cytotoxic C(2)-symmetric marine-derived bis(lactone) disorazole C(1), a highly convergent, modular strategy is employed featuring cyclization through an ambitious one-pot alkyne cross-metathesis/ring-closing metathesis self-assembly process. WILEY-VCH Verlag 2015-06-08 2015-04-29 /pmc/articles/PMC4517162/ /pubmed/25926364 http://dx.doi.org/10.1002/anie.201501922 Text en © 2015 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Ralston, Kevin J
Ramstadius, H Clinton
Brewster, Richard C
Niblock, Helen S
Hulme, Alison N
Self-Assembly of Disorazole C(1) through a One-Pot Alkyne Metathesis Homodimerization Strategy**
title Self-Assembly of Disorazole C(1) through a One-Pot Alkyne Metathesis Homodimerization Strategy**
title_full Self-Assembly of Disorazole C(1) through a One-Pot Alkyne Metathesis Homodimerization Strategy**
title_fullStr Self-Assembly of Disorazole C(1) through a One-Pot Alkyne Metathesis Homodimerization Strategy**
title_full_unstemmed Self-Assembly of Disorazole C(1) through a One-Pot Alkyne Metathesis Homodimerization Strategy**
title_short Self-Assembly of Disorazole C(1) through a One-Pot Alkyne Metathesis Homodimerization Strategy**
title_sort self-assembly of disorazole c(1) through a one-pot alkyne metathesis homodimerization strategy**
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517162/
https://www.ncbi.nlm.nih.gov/pubmed/25926364
http://dx.doi.org/10.1002/anie.201501922
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