19669-82-0

Upstream product

• 19973-76-3 (+/-)-oestrone 
• 75863-04-6 rac-3-Methoxy-6,7:8,9-diseco-1,3,5⁽¹⁰⁾,7-oestratetraen-9,17-dion 
• 52289-54-0 4-methoxysalicylaldehyde 
• 27060-75-9 4-bromo-3-methylanisole 
• 17447-60-8 dimethyl 2-vinylcyclopropane-1,1-dicarboxylate 
• 63518-90-1 (2Ξ,3SR)-2-Methyl-3-vinylcyclopentan-1-on 
• 57069-78-0 <(1SR,2Ξ)-2-Methyl-3-oxocyclopentyl>essigsaeure-methylester 
• 75863-25-1 2-Trimethylsilyl-1-(4-methoxy-2-methylphenyl)prop-2-en-1-on 
• 80868-66-2 1-(4-Methoxy-2-methylphenyl)prop-2-en-1-on 
• 80868-64-0 1-(4-Methoxy-2-methylphenyl)prop-2-en-1-ol 
• 75863-11-5 2-<(6Ξ,4SR)-6-Methyl-1,4-dioxaspiro<4.4>non-7-yl>ethanol 
• 75863-12-6 (6Ξ,7SR)-6-Methyl-7-vinyl-1,4-dioxaspiro<4.4>nonan 
• 75863-10-4 <(6Ξ,7SR)-6-Methyl-1,4-dioxaspiro<4.4>non-7-yl>essigsaeure-methylester 
• 80868-65-1 2-Trimethylsilyl-1-(4-methoxy-2-methylphenyl)prop-2-en-1-ol 

Downstream Products

• 1474-52-8 17β-oestradiol diacetate 
• 1743-60-8 17-β-estradiol 17-acetate 
• 24381-12-2 2-iodo-17β-oestradiol 
• 15833-07-5 2-bromo-17β-oestradiol 
• 88847-87-4 2-chloro-17β-oestradiol 

Relevant academic research and scientific papers

A Total Synthesis of Estradiol and its 6,6-Dimethyl Analogue

A short, stereoselective synthesis of estradiol, and its 6,6-dimethyl analogue, was accomplished from non-steroidal starting materials.A key feature was the use of a benzothiophene unit to effect (i) the stereoselective formation of the required 8β-H c