1. Department of Pharmaceutical Sciences, Faculty of Pharmacy, Keio University, Tokyo, Japan;2. Department of Chemistry, Graduate School of SIGMA Clermont, Aubiere Cedex, France
Abstract:
Wogonin and astringin were synthesized from inexpensive chrysin and piceid in short steps. The key feature of these syntheses is site-selective transformation. The target molecules were obtained in 27 and 62% yields from the starting materials, respectively.