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Germacrene B – a central intermediate in sesquiterpene biosynthesis

Germacranes are important intermediates in the biosynthesis of eudesmane and guaiane sesquiterpenes. After their initial formation from farnesyl diphosphate, these neutral intermediates can become reprotonated for a second cyclisation to reach the bicyclic eudesmane and guaiane skeletons. This revie...

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Autores principales: Xu, Houchao, Dickschat, Jeroen S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972886/
https://www.ncbi.nlm.nih.gov/pubmed/36865023
http://dx.doi.org/10.3762/bjoc.19.18
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author Xu, Houchao
Dickschat, Jeroen S
author_facet Xu, Houchao
Dickschat, Jeroen S
author_sort Xu, Houchao
collection PubMed
description Germacranes are important intermediates in the biosynthesis of eudesmane and guaiane sesquiterpenes. After their initial formation from farnesyl diphosphate, these neutral intermediates can become reprotonated for a second cyclisation to reach the bicyclic eudesmane and guaiane skeletons. This review summarises the accumulated knowledge on eudesmane and guaiane sesquiterpene hydrocarbons and alcohols that potentially arise from the achiral sesquiterpene hydrocarbon germacrene B. Not only compounds isolated from natural sources, but also synthetic compounds are dicussed, with the aim to give a rationale for the structural assignment for each compound. A total number of 64 compounds is presented, with 131 cited references.
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spelling pubmed-99728862023-03-01 Germacrene B – a central intermediate in sesquiterpene biosynthesis Xu, Houchao Dickschat, Jeroen S Beilstein J Org Chem Review Germacranes are important intermediates in the biosynthesis of eudesmane and guaiane sesquiterpenes. After their initial formation from farnesyl diphosphate, these neutral intermediates can become reprotonated for a second cyclisation to reach the bicyclic eudesmane and guaiane skeletons. This review summarises the accumulated knowledge on eudesmane and guaiane sesquiterpene hydrocarbons and alcohols that potentially arise from the achiral sesquiterpene hydrocarbon germacrene B. Not only compounds isolated from natural sources, but also synthetic compounds are dicussed, with the aim to give a rationale for the structural assignment for each compound. A total number of 64 compounds is presented, with 131 cited references. Beilstein-Institut 2023-02-20 /pmc/articles/PMC9972886/ /pubmed/36865023 http://dx.doi.org/10.3762/bjoc.19.18 Text en Copyright © 2023, Xu and Dickschat https://creativecommons.org/licenses/by/4.0/This is an open access article licensed under the terms of the Beilstein-Institut Open Access License Agreement (https://www.beilstein-journals.org/bjoc/terms/terms), which is identical to the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ). The reuse of material under this license requires that the author(s), source and license are credited. Third-party material in this article could be subject to other licenses (typically indicated in the credit line), and in this case, users are required to obtain permission from the license holder to reuse the material.
spellingShingle Review
Xu, Houchao
Dickschat, Jeroen S
Germacrene B – a central intermediate in sesquiterpene biosynthesis
title Germacrene B – a central intermediate in sesquiterpene biosynthesis
title_full Germacrene B – a central intermediate in sesquiterpene biosynthesis
title_fullStr Germacrene B – a central intermediate in sesquiterpene biosynthesis
title_full_unstemmed Germacrene B – a central intermediate in sesquiterpene biosynthesis
title_short Germacrene B – a central intermediate in sesquiterpene biosynthesis
title_sort germacrene b – a central intermediate in sesquiterpene biosynthesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9972886/
https://www.ncbi.nlm.nih.gov/pubmed/36865023
http://dx.doi.org/10.3762/bjoc.19.18
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