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Total syntheses of strained polycyclic terpenes
Terpenoids constitute a broad class of natural compounds with tremendous variability in structure and bioactivity, which resulted in a strong interest of the chemical community to this class of natural products over the last 150 years. The presence of strained small rings renders the terpenoid targe...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017437/ https://www.ncbi.nlm.nih.gov/pubmed/35388836 http://dx.doi.org/10.1039/d2cc00926a |
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author | Chesnokov, Gleb A. Gademann, Karl |
author_facet | Chesnokov, Gleb A. Gademann, Karl |
author_sort | Chesnokov, Gleb A. |
collection | PubMed |
description | Terpenoids constitute a broad class of natural compounds with tremendous variability in structure and bioactivity, which resulted in a strong interest of the chemical community to this class of natural products over the last 150 years. The presence of strained small rings renders the terpenoid targets interesting for chemical synthesis, due to limited number of available methods and stability issues. In this feature article, a number of recent examples of total syntheses of terpenoids with complex carbon frameworks featuring small rings are discussed. Specific emphasis is given to the new developments in strategical and tactical approaches to construction of such systems. |
format | Online Article Text |
id | pubmed-9017437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90174372022-06-01 Total syntheses of strained polycyclic terpenes Chesnokov, Gleb A. Gademann, Karl Chem Commun (Camb) Chemistry Terpenoids constitute a broad class of natural compounds with tremendous variability in structure and bioactivity, which resulted in a strong interest of the chemical community to this class of natural products over the last 150 years. The presence of strained small rings renders the terpenoid targets interesting for chemical synthesis, due to limited number of available methods and stability issues. In this feature article, a number of recent examples of total syntheses of terpenoids with complex carbon frameworks featuring small rings are discussed. Specific emphasis is given to the new developments in strategical and tactical approaches to construction of such systems. The Royal Society of Chemistry 2022-03-30 /pmc/articles/PMC9017437/ /pubmed/35388836 http://dx.doi.org/10.1039/d2cc00926a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Chesnokov, Gleb A. Gademann, Karl Total syntheses of strained polycyclic terpenes |
title | Total syntheses of strained polycyclic terpenes |
title_full | Total syntheses of strained polycyclic terpenes |
title_fullStr | Total syntheses of strained polycyclic terpenes |
title_full_unstemmed | Total syntheses of strained polycyclic terpenes |
title_short | Total syntheses of strained polycyclic terpenes |
title_sort | total syntheses of strained polycyclic terpenes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017437/ https://www.ncbi.nlm.nih.gov/pubmed/35388836 http://dx.doi.org/10.1039/d2cc00926a |
work_keys_str_mv | AT chesnokovgleba totalsynthesesofstrainedpolycyclicterpenes AT gademannkarl totalsynthesesofstrainedpolycyclicterpenes |