Efficient and stereoselective synthesis of sugar fused pyrano[3,2-]pyranones as anticancer agents

A highly stereoselective, efficient and facile route was achieved for the synthesis of novel and biochemically potent sugar fused pyrano[3,2- c ]pyranone derivatives starting from inexpensive, naturally occurring d -galactose and d -glucose. First, β- C -glycopyranosyl aldehydes were synthesized from these d -hexose sugars in six steps, with overall yields 41-55%. Next, two different 1- C -formyl glycals were synthesized from these β- C -glycopyranosyl aldehydes by treatment in basic conditions. The optimization of reaction conditions was carried out following reactions between 1- C -formyl galactal and 4-hydroxycoumarin. Next, 1- C -formyl galactal and 1- C -formyl glucal were treated with nine substituted 4-hydroxy coumarins at room temperature (25 °C) in ethyl acetate for ∼1-2 h in the presence of l -proline to obtain exclusively single diastereomers of pyrano[3,2- c ]pyranone derivatives in excellent yields. Four compounds were found to be active for the MCF-7 cancer cell line. The MTT assay, apoptosis assay and migration analysis showed significant death of the cancer cells induced by the synthesized compounds. A highly stereoselective, efficient and facile route was achieved for the synthesis of novel and biochemically potent sugar fused pyrano[3,2- c ]pyranone derivatives starting from inexpensive, naturally occurring d -galactose and d -glucose.