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Synthesis of glycosylcurcuminoids
Kunihiko Mohri1, Yuhya Watanabe, Yuki Yoshida
1Showa Pharmaceutical University, Tokyo, Japan. mohri@ac.shoyaku.ac.jp
Chemical & Pharmaceutical Bulletin
|November 6, 2003
Abstract:
Condensation of glycosylated arylaldehyde with acetylacetone-B(2)O(3) complex gave a corresponding diglycosylcurcuminoid, and a similar reaction using a mixture of arylaldehyde and glycosylarylaldehyde gave an unsymmetrical monoglycosylcurcuminoid, both as boron-complexes. The boron was removed from the complexes by heating in methanol, thus achieving the synthesis of di- and mono-glycosylcurcuminoids.