Synthetic Strategies and Tactics for Catechin and Related Polyphenols

Author:

Ohmori Ken,Suzuki Keisuke

Publisher

John Wiley & Sons, Ltd

Reference37 articles.

1. Asymmetric total synthesis of B-ring modified (-)-epicatechin gallate analogues and their modulation of β-lactam resistance in Staphylococcus aureus;Anderson;Tetrahedron,2005

2. Enantioselective synthesis of flavonoids. Part I. Polyoxygenated chalcone epoxides;Augustyn;Tetrahedron,1990

3. Flavan derivatives XVIII. Synthesis of hemiketals containing the peltogynol ring system: 3(3′)-hydroxyisochromano(4′,3′:2,3)chromans. Conversion of 2′-hydroxychalcones into flav-3-enes and its biosynthetic implications;Clark-Lewis;Australian Journal of Chemistry,1967

4. A fast assembly of (-)-epigallocatechin-3-gallate [(-)-EGCG] via intra- and inter-molecular Mitsunobu reaction;Ding;Chinese Journal of Chemistry,2006

5. Towards the synthesis of proanthocyanidins: half a century of innovation;Ferreira;Planta Medica,2011

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