Conversion of flavanones into chalcones in alkaline medium. Kinetic and spectroscopic studies

The conversion of flavanone and 7‐hydroxyflavanone in alkaline water and heavy water and of the same compounds and of 4′ ‐nitroflavanone in alkali‐methanolic media into the corresponding substituted chalcones was studied kinetically and spectroscopically. Treatment of kinetic data in this work and d...

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Publicado: 1991
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_08943230_v4_n5_p263_Nudelman
http://hdl.handle.net/20.500.12110/paper_08943230_v4_n5_p263_Nudelman
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spelling paper:paper_08943230_v4_n5_p263_Nudelman2023-06-08T15:47:49Z Conversion of flavanones into chalcones in alkaline medium. Kinetic and spectroscopic studies The conversion of flavanone and 7‐hydroxyflavanone in alkaline water and heavy water and of the same compounds and of 4′ ‐nitroflavanone in alkali‐methanolic media into the corresponding substituted chalcones was studied kinetically and spectroscopically. Treatment of kinetic data in this work and data for the reverse reaction determined previously allowed the estimation of the partial rate coefficients for each step and of the free‐energy changes for the three systems studied. To disentangle isotope effects, the conversion of [3‐D2]‐flavanone was also studied. The present results confirm a previously suggested mechanism for the spontaneous reaction and afford essential information that may contribute to a more detailed understanding of the mechanism of the enzyme‐catalysed reaction. Copyright © 1991 John Wiley & Sons Ltd. 1991 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_08943230_v4_n5_p263_Nudelman http://hdl.handle.net/20.500.12110/paper_08943230_v4_n5_p263_Nudelman
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description The conversion of flavanone and 7‐hydroxyflavanone in alkaline water and heavy water and of the same compounds and of 4′ ‐nitroflavanone in alkali‐methanolic media into the corresponding substituted chalcones was studied kinetically and spectroscopically. Treatment of kinetic data in this work and data for the reverse reaction determined previously allowed the estimation of the partial rate coefficients for each step and of the free‐energy changes for the three systems studied. To disentangle isotope effects, the conversion of [3‐D2]‐flavanone was also studied. The present results confirm a previously suggested mechanism for the spontaneous reaction and afford essential information that may contribute to a more detailed understanding of the mechanism of the enzyme‐catalysed reaction. Copyright © 1991 John Wiley & Sons Ltd.
title Conversion of flavanones into chalcones in alkaline medium. Kinetic and spectroscopic studies
spellingShingle Conversion of flavanones into chalcones in alkaline medium. Kinetic and spectroscopic studies
title_short Conversion of flavanones into chalcones in alkaline medium. Kinetic and spectroscopic studies
title_full Conversion of flavanones into chalcones in alkaline medium. Kinetic and spectroscopic studies
title_fullStr Conversion of flavanones into chalcones in alkaline medium. Kinetic and spectroscopic studies
title_full_unstemmed Conversion of flavanones into chalcones in alkaline medium. Kinetic and spectroscopic studies
title_sort conversion of flavanones into chalcones in alkaline medium. kinetic and spectroscopic studies
publishDate 1991
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_08943230_v4_n5_p263_Nudelman
http://hdl.handle.net/20.500.12110/paper_08943230_v4_n5_p263_Nudelman
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