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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...

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Autores principales: Nakamura, Akira, Mimaki, Kazuki, Tanigami, Ken-ichi, Maegawa, Tomohiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
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.
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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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