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An Improved and Practical Method for Synthesizing of α-Sanshools and Spilanthol
An efficient and practical route for the synthesis of α-sanshools and spilanthol is described herein. Several modifications of an existing method enabled the preparation of the (2E,6Z,8E,10E)-tetraene precursor of hydroxy-α-sanshool in good yield. A highly selective Wittig reaction employing newly s...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090093/ https://www.ncbi.nlm.nih.gov/pubmed/32258001 http://dx.doi.org/10.3389/fchem.2020.00187 |
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author | Nakamura, Akira Mimaki, Kazuki Tanigami, Ken-ichi Maegawa, Tomohiro |
author_facet | Nakamura, Akira Mimaki, Kazuki Tanigami, Ken-ichi Maegawa, Tomohiro |
author_sort | Nakamura, Akira |
collection | PubMed |
description | An efficient and practical route for the synthesis of α-sanshools and spilanthol is described herein. Several modifications of an existing method enabled the preparation of the (2E,6Z,8E,10E)-tetraene precursor of hydroxy-α-sanshool in good yield. A highly selective Wittig reaction employing newly synthesized phosphonium salt with low deliquescence and long-term stability yielded the desired Z-form tetraene. This improved methodology was shown to be applicable to the efficient synthesis of α-sanshool and spilanthol. |
format | Online Article Text |
id | pubmed-7090093 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70900932020-03-31 An Improved and Practical Method for Synthesizing of α-Sanshools and Spilanthol Nakamura, Akira Mimaki, Kazuki Tanigami, Ken-ichi Maegawa, Tomohiro Front Chem Chemistry An efficient and practical route for the synthesis of α-sanshools and spilanthol is described herein. Several modifications of an existing method enabled the preparation of the (2E,6Z,8E,10E)-tetraene precursor of hydroxy-α-sanshool in good yield. A highly selective Wittig reaction employing newly synthesized phosphonium salt with low deliquescence and long-term stability yielded the desired Z-form tetraene. This improved methodology was shown to be applicable to the efficient synthesis of α-sanshool and spilanthol. Frontiers Media S.A. 2020-03-17 /pmc/articles/PMC7090093/ /pubmed/32258001 http://dx.doi.org/10.3389/fchem.2020.00187 Text en Copyright © 2020 Nakamura, Mimaki, Tanigami and Maegawa. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Nakamura, Akira Mimaki, Kazuki Tanigami, Ken-ichi Maegawa, Tomohiro An Improved and Practical Method for Synthesizing of α-Sanshools and Spilanthol |
title | An Improved and Practical Method for Synthesizing of α-Sanshools and Spilanthol |
title_full | An Improved and Practical Method for Synthesizing of α-Sanshools and Spilanthol |
title_fullStr | An Improved and Practical Method for Synthesizing of α-Sanshools and Spilanthol |
title_full_unstemmed | An Improved and Practical Method for Synthesizing of α-Sanshools and Spilanthol |
title_short | An Improved and Practical Method for Synthesizing of α-Sanshools and Spilanthol |
title_sort | improved and practical method for synthesizing of α-sanshools and spilanthol |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090093/ https://www.ncbi.nlm.nih.gov/pubmed/32258001 http://dx.doi.org/10.3389/fchem.2020.00187 |
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