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Biogenetic space-guided synthesis of rearranged terpenoids

Natural product chemistry is constantly challenged by newly discovered, complex molecules. Elements of complexity arise from unprecedented frameworks, with a large amount of densely packed stereogenic centres and different functional groups along with a generally high oxidation state. As a prime exa...

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Detalles Bibliográficos
Autores principales: Alekseychuk, Mykhaylo, Heretsch, Philipp
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234310/
https://www.ncbi.nlm.nih.gov/pubmed/37162324
http://dx.doi.org/10.1039/d3cc01009k
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author Alekseychuk, Mykhaylo
Heretsch, Philipp
author_facet Alekseychuk, Mykhaylo
Heretsch, Philipp
author_sort Alekseychuk, Mykhaylo
collection PubMed
description Natural product chemistry is constantly challenged by newly discovered, complex molecules. Elements of complexity arise from unprecedented frameworks, with a large amount of densely packed stereogenic centres and different functional groups along with a generally high oxidation state. As a prime example, rearranged triterpenoids possess all these elements. For their total synthesis, a limit of what is considered sensible in terms of steps and yield is frequently reached. As an alternative, semisynthetic approaches have gained a great amount of attention in recent years. In this featured article, we present our and others' contributions towards the development of efficient and economic syntheses of complex terpenoid natural products and elaborate on the underlying rationale of biogenetic space-guided synthetic analysis.
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spelling pubmed-102343102023-06-02 Biogenetic space-guided synthesis of rearranged terpenoids Alekseychuk, Mykhaylo Heretsch, Philipp Chem Commun (Camb) Chemistry Natural product chemistry is constantly challenged by newly discovered, complex molecules. Elements of complexity arise from unprecedented frameworks, with a large amount of densely packed stereogenic centres and different functional groups along with a generally high oxidation state. As a prime example, rearranged triterpenoids possess all these elements. For their total synthesis, a limit of what is considered sensible in terms of steps and yield is frequently reached. As an alternative, semisynthetic approaches have gained a great amount of attention in recent years. In this featured article, we present our and others' contributions towards the development of efficient and economic syntheses of complex terpenoid natural products and elaborate on the underlying rationale of biogenetic space-guided synthetic analysis. The Royal Society of Chemistry 2023-05-10 /pmc/articles/PMC10234310/ /pubmed/37162324 http://dx.doi.org/10.1039/d3cc01009k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Alekseychuk, Mykhaylo
Heretsch, Philipp
Biogenetic space-guided synthesis of rearranged terpenoids
title Biogenetic space-guided synthesis of rearranged terpenoids
title_full Biogenetic space-guided synthesis of rearranged terpenoids
title_fullStr Biogenetic space-guided synthesis of rearranged terpenoids
title_full_unstemmed Biogenetic space-guided synthesis of rearranged terpenoids
title_short Biogenetic space-guided synthesis of rearranged terpenoids
title_sort biogenetic space-guided synthesis of rearranged terpenoids
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234310/
https://www.ncbi.nlm.nih.gov/pubmed/37162324
http://dx.doi.org/10.1039/d3cc01009k
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