890663-94-2

Upstream product

• 890663-84-0 Toluene-4-sulfonic acid (2R,6R)-6-((3S,8S,9S,10R,13S,14S,16S,17R)-3-benzyloxy-16-hydroxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methyl-heptyl ester 
• 512-04-9 diosgenin 
• 146333-24-6 3-O-benzyl diosgenin 
• 100-39-0 benzyl bromide 
• 890663-82-8 16-β,26-dihydroxyl cholesterol 
• 890663-90-8 Acetic acid (3S,8R,9S,10R,13S,14S)-3-benzyloxy-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-16-yl ester 
• 890663-86-2 (3S,8S,9S,10R,13S,14S,16S,17R)-3-Benzyloxy-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-16-ol 
• 890663-88-4 (3S,8S,9S,10R,13S,14S,17R)-3-Benzyloxy-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-1,2,3,4,7,8,9,10,11,12,13,14,15,17-tetradecahydro-cyclopenta[a]phenanthren-16-one 
• 890663-92-0 (3S,8R,9S,10R,13S,14S,17S)-3-Benzyloxy-17-((R)-1,5-dimethyl-hexyl)-17-hydroxy-10,13-dimethyl-1,2,3,4,7,8,9,10,11,12,13,14,15,17-tetradecahydro-cyclopenta[a]phenanthren-16-one 

Relevant academic research and scientific papers

A highly efficient synthesis of 22-deoxy-OSW-1 by utilizing the intact skeleton of diosgenin

22-Deoxy-OSW-1 (1), an analogue of OSW-1 with the potent anticancer activity, was synthesized by utilizing the intact skeleton of diosgenin in 11 steps in 13.7% overall yield. This synthesis demonstrated an effective and reasonable synthetic strategy for