Nicolaou_2010_J.Am.Chem.Soc_132_7540

Reference

Title : Total synthesis and biological evaluation of the resveratrol-derived polyphenol natural products hopeanol and hopeahainol A - Nicolaou_2010_J.Am.Chem.Soc_132_7540
Author(s) : Nicolaou KC , Kang Q , Wu TR , Lim CS , Chen DY
Ref : Journal of the American Chemical Society , 132 :7540 , 2010
Abstract :

The total synthesis and biological evaluation of the resveratrol-derived natural products hopeanol (2) and hopeahainol A (3) in their racemic and antipodal forms are described. The Friedel-Crafts-based synthetic strategy employed was developed from model studies that established the feasibility of constructing the C(7b) quaternary center through an intramolecular Friedel-Crafts reaction and a Grob-type fragmentation to introduce an obligatory olefinic bond in the growing molecule. The final stages of the synthesis involved an epoxide substrate and an intramolecular Friedel-Crafts reaction, followed by oxidation to afford, upon global deprotection, hopeahainol A (3). The latter was converted under basic conditions to hopeanol (2), whereas the reverse transformation, previously suggested as a step in the biosynthesis of hopeahainol A (3), was not observed under a variety of conditions. Biological evaluation of the synthesized compounds confirmed the reported acetylcholinesterase inhibitory activity of hopeahainol A (3) but not the reported cytotoxic potencies of hopeanol (2).

PubMedSearch : Nicolaou_2010_J.Am.Chem.Soc_132_7540
PubMedID: 20462209

Related information

Inhibitor Hopeahainol-A

Citations formats

Nicolaou KC, Kang Q, Wu TR, Lim CS, Chen DY (2010)
Total synthesis and biological evaluation of the resveratrol-derived polyphenol natural products hopeanol and hopeahainol A
Journal of the American Chemical Society 132 :7540

Nicolaou KC, Kang Q, Wu TR, Lim CS, Chen DY (2010)
Journal of the American Chemical Society 132 :7540