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Indole diterpenoid natural products as the inspiration for new synthetic methods and strategies
Indole terpenoids comprise a large class of natural products with diverse structural topologies and a broad range of biological activities. Accordingly, indole terpenoids have and continue to serve as attractive targets for chemical synthesis. Many synthetic efforts over the past few years have focu...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618777/ https://www.ncbi.nlm.nih.gov/pubmed/28970940 http://dx.doi.org/10.1039/c7sc01248a |
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author | Corsello, Michael A. Kim, Junyong Garg, Neil K. |
author_facet | Corsello, Michael A. Kim, Junyong Garg, Neil K. |
author_sort | Corsello, Michael A. |
collection | PubMed |
description | Indole terpenoids comprise a large class of natural products with diverse structural topologies and a broad range of biological activities. Accordingly, indole terpenoids have and continue to serve as attractive targets for chemical synthesis. Many synthetic efforts over the past few years have focused on a subclass of this family, the indole diterpenoids. This minireview showcases the role indole diterpenoids have played in inspiring the recent development of clever synthetic strategies, and new chemical reactions. |
format | Online Article Text |
id | pubmed-5618777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-56187772017-10-02 Indole diterpenoid natural products as the inspiration for new synthetic methods and strategies Corsello, Michael A. Kim, Junyong Garg, Neil K. Chem Sci Chemistry Indole terpenoids comprise a large class of natural products with diverse structural topologies and a broad range of biological activities. Accordingly, indole terpenoids have and continue to serve as attractive targets for chemical synthesis. Many synthetic efforts over the past few years have focused on a subclass of this family, the indole diterpenoids. This minireview showcases the role indole diterpenoids have played in inspiring the recent development of clever synthetic strategies, and new chemical reactions. Royal Society of Chemistry 2017-09-01 2017-06-27 /pmc/articles/PMC5618777/ /pubmed/28970940 http://dx.doi.org/10.1039/c7sc01248a Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Corsello, Michael A. Kim, Junyong Garg, Neil K. Indole diterpenoid natural products as the inspiration for new synthetic methods and strategies |
title | Indole diterpenoid natural products as the inspiration for new synthetic methods and strategies |
title_full | Indole diterpenoid natural products as the inspiration for new synthetic methods and strategies |
title_fullStr | Indole diterpenoid natural products as the inspiration for new synthetic methods and strategies |
title_full_unstemmed | Indole diterpenoid natural products as the inspiration for new synthetic methods and strategies |
title_short | Indole diterpenoid natural products as the inspiration for new synthetic methods and strategies |
title_sort | indole diterpenoid natural products as the inspiration for new synthetic methods and strategies |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618777/ https://www.ncbi.nlm.nih.gov/pubmed/28970940 http://dx.doi.org/10.1039/c7sc01248a |
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