abstract |
The present invention relates to a compound of general formula (A). The invention provides asynthesis of new 4 β -amidotriazole linked podophyllotoxin derivatives of general formulae 8a-z to 9a-z useful as potential anticancer agents against human cancer cell lines and process for the preparation thereof. Wherein n = 0,1 and R 1 -R 5 = [H, CI, F, CH 3 , OCH 3 , 3,4(-OCH 2 O-), CF 3 , OCF 3 , m-OC 6 H 5 , OH] |