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The pinene scaffold: its occurrence, chemistry, synthetic utility, and pharmacological importance

Plant-based secondary metabolites have been a major source of drug discovery and inspiration for new generations of drugs. Plants offer a wide variety of compound classes, including alkaloids, terpenes, flavonoids, and glycosides, with different molecular architectures (fused bridgehead, bi- and pol...

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Detalles Bibliográficos
Autores principales: Nyamwihura, Rogers J., Ogungbe, Ifedayo Victor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9003397/
https://www.ncbi.nlm.nih.gov/pubmed/35425061
http://dx.doi.org/10.1039/d2ra00423b
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author Nyamwihura, Rogers J.
Ogungbe, Ifedayo Victor
author_facet Nyamwihura, Rogers J.
Ogungbe, Ifedayo Victor
author_sort Nyamwihura, Rogers J.
collection PubMed
description Plant-based secondary metabolites have been a major source of drug discovery and inspiration for new generations of drugs. Plants offer a wide variety of compound classes, including alkaloids, terpenes, flavonoids, and glycosides, with different molecular architectures (fused bridgehead, bi- and polycyclic, spirocyclic, polycyclic, and acyclic). The diversity, abundance, and accessibility of plant metabolites make plants an attractive source of human and animal medicine. Even though the pinene scaffold is abundant in nature and has historical use in traditional medicine, pinene and pinene-derived compounds have not been comprehensively studied for medicinal applications. This review provides insight into the utility of the pinene scaffold as a crucial building block of important natural and synthetic products and as a chiral reagent in the asymmetric synthesis of important compounds.
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spelling pubmed-90033972022-04-13 The pinene scaffold: its occurrence, chemistry, synthetic utility, and pharmacological importance Nyamwihura, Rogers J. Ogungbe, Ifedayo Victor RSC Adv Chemistry Plant-based secondary metabolites have been a major source of drug discovery and inspiration for new generations of drugs. Plants offer a wide variety of compound classes, including alkaloids, terpenes, flavonoids, and glycosides, with different molecular architectures (fused bridgehead, bi- and polycyclic, spirocyclic, polycyclic, and acyclic). The diversity, abundance, and accessibility of plant metabolites make plants an attractive source of human and animal medicine. Even though the pinene scaffold is abundant in nature and has historical use in traditional medicine, pinene and pinene-derived compounds have not been comprehensively studied for medicinal applications. This review provides insight into the utility of the pinene scaffold as a crucial building block of important natural and synthetic products and as a chiral reagent in the asymmetric synthesis of important compounds. The Royal Society of Chemistry 2022-04-12 /pmc/articles/PMC9003397/ /pubmed/35425061 http://dx.doi.org/10.1039/d2ra00423b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Nyamwihura, Rogers J.
Ogungbe, Ifedayo Victor
The pinene scaffold: its occurrence, chemistry, synthetic utility, and pharmacological importance
title The pinene scaffold: its occurrence, chemistry, synthetic utility, and pharmacological importance
title_full The pinene scaffold: its occurrence, chemistry, synthetic utility, and pharmacological importance
title_fullStr The pinene scaffold: its occurrence, chemistry, synthetic utility, and pharmacological importance
title_full_unstemmed The pinene scaffold: its occurrence, chemistry, synthetic utility, and pharmacological importance
title_short The pinene scaffold: its occurrence, chemistry, synthetic utility, and pharmacological importance
title_sort pinene scaffold: its occurrence, chemistry, synthetic utility, and pharmacological importance
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9003397/
https://www.ncbi.nlm.nih.gov/pubmed/35425061
http://dx.doi.org/10.1039/d2ra00423b
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