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Enantioselective Total Synthesis of (R,R)-Blumenol B and d(9)-(R,R)-Blumenol B

C(13)-norisoprenoids are of particular importance to grapes and wines, as these molecules influence wine aroma and have been shown to significantly contribute to the distinct character of various wine varieties. Blumenol B is a putative precursor to a number of important wine aroma compounds, includ...

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Detalles Bibliográficos
Autores principales: Tan, Shi Min, Rees, Shaun W. P., Jelley, Rebecca E., Wang, Jin, Fedrizzi, Bruno, Barker, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9655556/
https://www.ncbi.nlm.nih.gov/pubmed/36364120
http://dx.doi.org/10.3390/molecules27217294
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author Tan, Shi Min
Rees, Shaun W. P.
Jelley, Rebecca E.
Wang, Jin
Fedrizzi, Bruno
Barker, David
author_facet Tan, Shi Min
Rees, Shaun W. P.
Jelley, Rebecca E.
Wang, Jin
Fedrizzi, Bruno
Barker, David
author_sort Tan, Shi Min
collection PubMed
description C(13)-norisoprenoids are of particular importance to grapes and wines, as these molecules influence wine aroma and have been shown to significantly contribute to the distinct character of various wine varieties. Blumenol B is a putative precursor to a number of important wine aroma compounds, including the well-known compounds theaspirone and vitispirane. The enantioselective synthesis of (R,R)-blumenol B from commercially available 4-oxoisophorone was achieved using a short and easily scaleable route, which was then successfully applied to the synthesis of poly-deuterated d9-blumenol B.
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spelling pubmed-96555562022-11-15 Enantioselective Total Synthesis of (R,R)-Blumenol B and d(9)-(R,R)-Blumenol B Tan, Shi Min Rees, Shaun W. P. Jelley, Rebecca E. Wang, Jin Fedrizzi, Bruno Barker, David Molecules Article C(13)-norisoprenoids are of particular importance to grapes and wines, as these molecules influence wine aroma and have been shown to significantly contribute to the distinct character of various wine varieties. Blumenol B is a putative precursor to a number of important wine aroma compounds, including the well-known compounds theaspirone and vitispirane. The enantioselective synthesis of (R,R)-blumenol B from commercially available 4-oxoisophorone was achieved using a short and easily scaleable route, which was then successfully applied to the synthesis of poly-deuterated d9-blumenol B. MDPI 2022-10-27 /pmc/articles/PMC9655556/ /pubmed/36364120 http://dx.doi.org/10.3390/molecules27217294 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tan, Shi Min
Rees, Shaun W. P.
Jelley, Rebecca E.
Wang, Jin
Fedrizzi, Bruno
Barker, David
Enantioselective Total Synthesis of (R,R)-Blumenol B and d(9)-(R,R)-Blumenol B
title Enantioselective Total Synthesis of (R,R)-Blumenol B and d(9)-(R,R)-Blumenol B
title_full Enantioselective Total Synthesis of (R,R)-Blumenol B and d(9)-(R,R)-Blumenol B
title_fullStr Enantioselective Total Synthesis of (R,R)-Blumenol B and d(9)-(R,R)-Blumenol B
title_full_unstemmed Enantioselective Total Synthesis of (R,R)-Blumenol B and d(9)-(R,R)-Blumenol B
title_short Enantioselective Total Synthesis of (R,R)-Blumenol B and d(9)-(R,R)-Blumenol B
title_sort enantioselective total synthesis of (r,r)-blumenol b and d(9)-(r,r)-blumenol b
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9655556/
https://www.ncbi.nlm.nih.gov/pubmed/36364120
http://dx.doi.org/10.3390/molecules27217294
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