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Isolation of the first C-2 addition products of anthocyanins

โœ Scribed by Yinrong Lu; L.Yeap Foo; Herbert Wong

Publisher
Elsevier Science
Year
2002
Tongue
French
Weight
111 KB
Volume
43
Category
Article
ISSN
0040-4039

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โœฆ Synopsis

Addition of anthocyanins with nucleophilic agents normally occurs at the C-4 centre and the isolation of C-2 adducts between acetone and cyanidin-3-and delphinidin-3-rutinosides is the first definitive demonstration of the reactivity of this carbon site. These C-2 addition products were isolated as diastereoisomers and their chemical structures elucidated by 1D and 2D NMR spectroscopy.

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