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Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol

The xishacorene natural products are structurally unique apolar diterpenoids that feature a bicyclo[3.3.1] framework. These secondary metabolites likely arise from the well-studied, structurally related diterpenoid fuscol. In this manuscript, we describe the conversion of fuscol to xishacorenes A, B...

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Autores principales: Rovira, Alexander R., Müller, Nicolas, Deng, Weiwen, Ndubaku, Chudi, Sarpong, Richmond
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761873/
https://www.ncbi.nlm.nih.gov/pubmed/31588327
http://dx.doi.org/10.1039/c9sc02572c
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author Rovira, Alexander R.
Müller, Nicolas
Deng, Weiwen
Ndubaku, Chudi
Sarpong, Richmond
author_facet Rovira, Alexander R.
Müller, Nicolas
Deng, Weiwen
Ndubaku, Chudi
Sarpong, Richmond
author_sort Rovira, Alexander R.
collection PubMed
description The xishacorene natural products are structurally unique apolar diterpenoids that feature a bicyclo[3.3.1] framework. These secondary metabolites likely arise from the well-studied, structurally related diterpenoid fuscol. In this manuscript, we describe the conversion of fuscol to xishacorenes A, B, and C, as well as a previously unreported congener, which we have named xishacorene D. In addition, we describe immunomodulatory activity studies of the xishacorenes, a structurally related analogue, and fuscol. These studies were aided by an accurate determination of the physical properties (e.g., molar extinction coefficient) of the highly apolar xishacorenes.
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spelling pubmed-67618732019-10-04 Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol Rovira, Alexander R. Müller, Nicolas Deng, Weiwen Ndubaku, Chudi Sarpong, Richmond Chem Sci Chemistry The xishacorene natural products are structurally unique apolar diterpenoids that feature a bicyclo[3.3.1] framework. These secondary metabolites likely arise from the well-studied, structurally related diterpenoid fuscol. In this manuscript, we describe the conversion of fuscol to xishacorenes A, B, and C, as well as a previously unreported congener, which we have named xishacorene D. In addition, we describe immunomodulatory activity studies of the xishacorenes, a structurally related analogue, and fuscol. These studies were aided by an accurate determination of the physical properties (e.g., molar extinction coefficient) of the highly apolar xishacorenes. Royal Society of Chemistry 2019-07-03 /pmc/articles/PMC6761873/ /pubmed/31588327 http://dx.doi.org/10.1039/c9sc02572c Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Rovira, Alexander R.
Müller, Nicolas
Deng, Weiwen
Ndubaku, Chudi
Sarpong, Richmond
Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol
title Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol
title_full Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol
title_fullStr Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol
title_full_unstemmed Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol
title_short Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol
title_sort bio-inspired synthesis of xishacorenes a, b, and c, and a new congener from fuscol
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761873/
https://www.ncbi.nlm.nih.gov/pubmed/31588327
http://dx.doi.org/10.1039/c9sc02572c
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