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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-9655556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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