84133-01-7

Upstream product

• 84133-00-6 2α-methyl-2β-<4,8-dimethyl-5-(ethylenedioxy)-7-nonenyl>-5α-(hydroxymethyl)-1,4-dioxane 
• 98-59-9 p-toluenesulfonyl chloride 
• 5978-08-5 1-chloro-4-(1,3-dioxolane)-n-pentane 
• 2570-68-5 6-oxo-2-methyl-heptanoic acid 
• 2570-90-3 6-oxo-2-methyl-heptanoic acid methyl ester 
• 50585-10-9 3-methyl-2-butenyllithium 
• 84132-93-4 methyl 2,6-dimethyl-6,7-epoxyheptanoate 
• 84132-92-3 2-Methyl-2-(4-oxo-pentyl)-malonic acid 
• 84132-94-5 methyl 2,6-dimethyl-6-(alloxy)-7-hydroxyheptanoate 
• 84132-96-7 methyl 2,6-dimethyl-6-<(2,3-epoxypropyl)oxy>-7-hydroxyheptanoate 
• 84132-99-0 2α-methyl-2β-(4,8-dimethyl-5-oxo-7-nonenyl)-5α-(hydroxymethyl)-1,4-dioxane 
• 84132-91-2 2-Methyl-2-[3-(2-methyl-[1,3]dioxolan-2-yl)-propyl]-malonic acid diethyl ester 
• 84173-73-9 2-Methyl-5-[(2R,5R)-2-methyl-5-(tetrahydro-pyran-2-yloxymethyl)-[1,4]dioxan-2-yl]-pentanoic acid 
• 84132-97-8 2α-methyl-2β-(4-carbomethoxypentyl)-5α-(hydroxymethyl)-1,4-dioxane 

Relevant academic research and scientific papers

Synthesis and Biological Activity of Zoapatanol Analogues

Dioxane analogues of the biologically active 3,6-oxido derivative (III) of zoapatanol (I) having substituents at the C-2 and C-5 positions, but lacking the ethano bridge, were evaluated for luteolytic and postcoital antifertility activity in the guinea pi