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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)...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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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. |
format | Online Article Text |
id | pubmed-5488202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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