In this study, a novel route to （-）-limonidilactone analogues 10, 11 by way of stereoselective reaction of andrographolide （5） from 8, 9 was reported. The anti-tumor and a-glucosidsae inhibition activities of some...In this study, a novel route to （-）-limonidilactone analogues 10, 11 by way of stereoselective reaction of andrographolide （5） from 8, 9 was reported. The anti-tumor and a-glucosidsae inhibition activities of some synthetic compounds were screened.展开更多
基金Project supported by the National Natural Science Foundation of China （No. 20902086）, and China Postdoctoral Science Foundation （No, 20080430864）.
文摘In this study, a novel route to （-）-limonidilactone analogues 10, 11 by way of stereoselective reaction of andrographolide （5） from 8, 9 was reported. The anti-tumor and a-glucosidsae inhibition activities of some synthetic compounds were screened.
