Abstract
More than five thousand naturally occurring flavonoids are known to exist. In this paper, we review the synthesis and transformation of flavan, flavone, flavonol, proanthocyanidin, anthocyanin, and related compounds on the basis of new and conceptual methodologies that have arisen in the last decade (2000-2010). We especially focus on new skeleton formations and the synthesis of flavonoid glycosides
Keywords: Anthocyanin, flavonoid, glycosyl flavone, organic synthesis, polyphenol, proanthocyanidin, pyranoanthocyanin, supramolecule, polyphenolic compounds, malonyl-CoA, flavonoid moieties, metalloanthocyanin
Current Organic Chemistry
Title: Recent Progress in the Synthesis of Flavonoids: From Monomers to Supra-Complex Molecules
Volume: 15 Issue: 15
Author(s): Kin-ichi Oyama, Kumi Yoshida and Tadao Kondo
Affiliation:
Keywords: Anthocyanin, flavonoid, glycosyl flavone, organic synthesis, polyphenol, proanthocyanidin, pyranoanthocyanin, supramolecule, polyphenolic compounds, malonyl-CoA, flavonoid moieties, metalloanthocyanin
Abstract: More than five thousand naturally occurring flavonoids are known to exist. In this paper, we review the synthesis and transformation of flavan, flavone, flavonol, proanthocyanidin, anthocyanin, and related compounds on the basis of new and conceptual methodologies that have arisen in the last decade (2000-2010). We especially focus on new skeleton formations and the synthesis of flavonoid glycosides
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Cite this article as:
Oyama Kin-ichi, Yoshida Kumi and Kondo Tadao, Recent Progress in the Synthesis of Flavonoids: From Monomers to Supra-Complex Molecules, Current Organic Chemistry 2011; 15 (15) . https://dx.doi.org/10.2174/138527211796367354
DOI https://dx.doi.org/10.2174/138527211796367354 |
Print ISSN 1385-2728 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5348 |
Call for Papers in Thematic Issues
Catalytic C-H bond activation as a tool for functionalization of heterocycles
The major topic is the functionalization of heterocycles through catalyzed C-H bond activation. The strategies based on C-H activation not only provide straightforward formation of C-C or C-X bonds but, more importantly, allow for the avoidance of pre-functionalization of one or two of the cross-coupling partners. The beneficial impact of ...read more
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