Conversion of flavonol glycoside to anthocyanin: an interpretation of the oxidation–reduction relationship of biosynthetic flavonoid-intermediates

An efficient conversion of rutin to the corresponding anthocyanin, cyanidin 3-O-rutinoside, was established. Clemmensen-type reduction of rutin gave a mixture of flav-2-en-3-ol and two flav-3-en-3-ols, which were easily oxidised by air to give the anthocyanin. The interconversion reactions of these...

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Detalles Bibliográficos
Autores principales: Oyama, Kin-ichi, Kimura, Yuki, Iuchi, Satoru, Koga, Nobuaki, Yoshida, Kumi, Kondo, Tadao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072432/
https://www.ncbi.nlm.nih.gov/pubmed/35527956
http://dx.doi.org/10.1039/c9ra06986k
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author Oyama, Kin-ichi
Kimura, Yuki
Iuchi, Satoru
Koga, Nobuaki
Yoshida, Kumi
Kondo, Tadao
author_facet Oyama, Kin-ichi
Kimura, Yuki
Iuchi, Satoru
Koga, Nobuaki
Yoshida, Kumi
Kondo, Tadao
author_sort Oyama, Kin-ichi
collection PubMed
description An efficient conversion of rutin to the corresponding anthocyanin, cyanidin 3-O-rutinoside, was established. Clemmensen-type reduction of rutin gave a mixture of flav-2-en-3-ol and two flav-3-en-3-ols, which were easily oxidised by air to give the anthocyanin. The interconversion reactions of these flavonoids provide insight into their biosynthetic pathway.
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spelling pubmed-90724322022-05-06 Conversion of flavonol glycoside to anthocyanin: an interpretation of the oxidation–reduction relationship of biosynthetic flavonoid-intermediates Oyama, Kin-ichi Kimura, Yuki Iuchi, Satoru Koga, Nobuaki Yoshida, Kumi Kondo, Tadao RSC Adv Chemistry An efficient conversion of rutin to the corresponding anthocyanin, cyanidin 3-O-rutinoside, was established. Clemmensen-type reduction of rutin gave a mixture of flav-2-en-3-ol and two flav-3-en-3-ols, which were easily oxidised by air to give the anthocyanin. The interconversion reactions of these flavonoids provide insight into their biosynthetic pathway. The Royal Society of Chemistry 2019-10-03 /pmc/articles/PMC9072432/ /pubmed/35527956 http://dx.doi.org/10.1039/c9ra06986k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Oyama, Kin-ichi
Kimura, Yuki
Iuchi, Satoru
Koga, Nobuaki
Yoshida, Kumi
Kondo, Tadao
Conversion of flavonol glycoside to anthocyanin: an interpretation of the oxidation–reduction relationship of biosynthetic flavonoid-intermediates
title Conversion of flavonol glycoside to anthocyanin: an interpretation of the oxidation–reduction relationship of biosynthetic flavonoid-intermediates
title_full Conversion of flavonol glycoside to anthocyanin: an interpretation of the oxidation–reduction relationship of biosynthetic flavonoid-intermediates
title_fullStr Conversion of flavonol glycoside to anthocyanin: an interpretation of the oxidation–reduction relationship of biosynthetic flavonoid-intermediates
title_full_unstemmed Conversion of flavonol glycoside to anthocyanin: an interpretation of the oxidation–reduction relationship of biosynthetic flavonoid-intermediates
title_short Conversion of flavonol glycoside to anthocyanin: an interpretation of the oxidation–reduction relationship of biosynthetic flavonoid-intermediates
title_sort conversion of flavonol glycoside to anthocyanin: an interpretation of the oxidation–reduction relationship of biosynthetic flavonoid-intermediates
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072432/
https://www.ncbi.nlm.nih.gov/pubmed/35527956
http://dx.doi.org/10.1039/c9ra06986k
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