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Communic Acids: Occurrence, Properties and Use as Chirons for the Synthesis of Bioactive Compounds

Communic acids are diterpenes with labdane skeletons found in many plant species, mainly conifers, predominating in the genus Juniperus (fam. Cupresaceae). In this review we briefly describe their distribution and different biological activities (anti- bacterial, antitumoral, hypolipidemic, relaxing...

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Detalles Bibliográficos
Autores principales: Barrero, Alejandro F., Herrador, M. Mar, Arteaga, Pilar, Arteaga, Jesús F., Arteaga, Alejandro F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268269/
https://www.ncbi.nlm.nih.gov/pubmed/22310167
http://dx.doi.org/10.3390/molecules17021448
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author Barrero, Alejandro F.
Herrador, M. Mar
Arteaga, Pilar
Arteaga, Jesús F.
Arteaga, Alejandro F.
author_facet Barrero, Alejandro F.
Herrador, M. Mar
Arteaga, Pilar
Arteaga, Jesús F.
Arteaga, Alejandro F.
author_sort Barrero, Alejandro F.
collection PubMed
description Communic acids are diterpenes with labdane skeletons found in many plant species, mainly conifers, predominating in the genus Juniperus (fam. Cupresaceae). In this review we briefly describe their distribution and different biological activities (anti- bacterial, antitumoral, hypolipidemic, relaxing smooth muscle, etc.). This paper also includes a detailed explanation of their use as chiral building blocks for the synthesis of bioactive natural products. Among other uses, communic acids have proven useful as chirons for the synthesis of quassinoids (formal), abietane antioxidants, ambrox and other perfume fixatives, podolactone herbicides, etc., featuring shorter and more efficient processes.
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spelling pubmed-62682692018-12-10 Communic Acids: Occurrence, Properties and Use as Chirons for the Synthesis of Bioactive Compounds Barrero, Alejandro F. Herrador, M. Mar Arteaga, Pilar Arteaga, Jesús F. Arteaga, Alejandro F. Molecules Review Communic acids are diterpenes with labdane skeletons found in many plant species, mainly conifers, predominating in the genus Juniperus (fam. Cupresaceae). In this review we briefly describe their distribution and different biological activities (anti- bacterial, antitumoral, hypolipidemic, relaxing smooth muscle, etc.). This paper also includes a detailed explanation of their use as chiral building blocks for the synthesis of bioactive natural products. Among other uses, communic acids have proven useful as chirons for the synthesis of quassinoids (formal), abietane antioxidants, ambrox and other perfume fixatives, podolactone herbicides, etc., featuring shorter and more efficient processes. MDPI 2012-02-06 /pmc/articles/PMC6268269/ /pubmed/22310167 http://dx.doi.org/10.3390/molecules17021448 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Barrero, Alejandro F.
Herrador, M. Mar
Arteaga, Pilar
Arteaga, Jesús F.
Arteaga, Alejandro F.
Communic Acids: Occurrence, Properties and Use as Chirons for the Synthesis of Bioactive Compounds
title Communic Acids: Occurrence, Properties and Use as Chirons for the Synthesis of Bioactive Compounds
title_full Communic Acids: Occurrence, Properties and Use as Chirons for the Synthesis of Bioactive Compounds
title_fullStr Communic Acids: Occurrence, Properties and Use as Chirons for the Synthesis of Bioactive Compounds
title_full_unstemmed Communic Acids: Occurrence, Properties and Use as Chirons for the Synthesis of Bioactive Compounds
title_short Communic Acids: Occurrence, Properties and Use as Chirons for the Synthesis of Bioactive Compounds
title_sort communic acids: occurrence, properties and use as chirons for the synthesis of bioactive compounds
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268269/
https://www.ncbi.nlm.nih.gov/pubmed/22310167
http://dx.doi.org/10.3390/molecules17021448
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