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Modular Synthesis of Diverse Natural Product‐Like Macrocycles: Discovery of Hits with Antimycobacterial Activity

A modular synthetic approach was developed in which variation of the triplets of building blocks used enabled systematic variation of the macrocyclic scaffolds prepared. The approach was demonstrated in the synthesis of 17 diverse natural product‐like macrocyclic scaffolds of varied (12–20‐membered)...

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Detalles Bibliográficos
Autores principales: Dow, Mark, Marchetti, Francesco, Abrahams, Katherine A., Vaz, Luis, Besra, Gurdyal S., Warriner, Stuart, Nelson, Adam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488202/
https://www.ncbi.nlm.nih.gov/pubmed/28374952
http://dx.doi.org/10.1002/chem.201701150
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author Dow, Mark
Marchetti, Francesco
Abrahams, Katherine A.
Vaz, Luis
Besra, Gurdyal S.
Warriner, Stuart
Nelson, Adam
author_facet Dow, Mark
Marchetti, Francesco
Abrahams, Katherine A.
Vaz, Luis
Besra, Gurdyal S.
Warriner, Stuart
Nelson, Adam
author_sort Dow, Mark
collection PubMed
description A modular synthetic approach was developed in which variation of the triplets of building blocks used enabled systematic variation of the macrocyclic scaffolds prepared. The approach was demonstrated in the synthesis of 17 diverse natural product‐like macrocyclic scaffolds of varied (12–20‐membered) ring size. The biological relevance of the chemical space explored was demonstrated through the discovery of a series of macrocycles with significant antimycobacterial activity.
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spelling pubmed-54882022017-07-13 Modular Synthesis of Diverse Natural Product‐Like Macrocycles: Discovery of Hits with Antimycobacterial Activity Dow, Mark Marchetti, Francesco Abrahams, Katherine A. Vaz, Luis Besra, Gurdyal S. Warriner, Stuart Nelson, Adam Chemistry Communications A modular synthetic approach was developed in which variation of the triplets of building blocks used enabled systematic variation of the macrocyclic scaffolds prepared. The approach was demonstrated in the synthesis of 17 diverse natural product‐like macrocyclic scaffolds of varied (12–20‐membered) ring size. The biological relevance of the chemical space explored was demonstrated through the discovery of a series of macrocycles with significant antimycobacterial activity. John Wiley and Sons Inc. 2017-05-02 2017-05-29 /pmc/articles/PMC5488202/ /pubmed/28374952 http://dx.doi.org/10.1002/chem.201701150 Text en © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Dow, Mark
Marchetti, Francesco
Abrahams, Katherine A.
Vaz, Luis
Besra, Gurdyal S.
Warriner, Stuart
Nelson, Adam
Modular Synthesis of Diverse Natural Product‐Like Macrocycles: Discovery of Hits with Antimycobacterial Activity
title Modular Synthesis of Diverse Natural Product‐Like Macrocycles: Discovery of Hits with Antimycobacterial Activity
title_full Modular Synthesis of Diverse Natural Product‐Like Macrocycles: Discovery of Hits with Antimycobacterial Activity
title_fullStr Modular Synthesis of Diverse Natural Product‐Like Macrocycles: Discovery of Hits with Antimycobacterial Activity
title_full_unstemmed Modular Synthesis of Diverse Natural Product‐Like Macrocycles: Discovery of Hits with Antimycobacterial Activity
title_short Modular Synthesis of Diverse Natural Product‐Like Macrocycles: Discovery of Hits with Antimycobacterial Activity
title_sort modular synthesis of diverse natural product‐like macrocycles: discovery of hits with antimycobacterial activity
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5488202/
https://www.ncbi.nlm.nih.gov/pubmed/28374952
http://dx.doi.org/10.1002/chem.201701150
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