944797-06-2

Upstream product

• 59974-82-2 (1S,3aS,7aS)-1-(1,1-dimethylethoxy)octahydro-7a-methyl-5H-inden-5-one 
• 944797-03-9 (1'S,3a'S,6'R,7a'S)-1'-(1,1-dimethylethoxy)octahydro-7'a-methyl-6'-[(7R)-7-(phenylmethoxy)-2-octenyl]-spiro[1,3-dioxolane-2,5'-[5H]indene] 
• 944797-02-8 (1S,3aS,6R,7aS)-1-(1,1-dimethylethoxy)octahydro-7a-methyl-6-[(7R)-7-(phenylmethoxy)-2-octenyl]-5H-inden-5-one 
• 944797-01-7 (1S,3aS,6R,7aS)-1-(1,1-dimethylethoxy)octahydro-7a-methyl-6-(prop-2-enyl)-5H-inden-5-one 
• 944797-00-6 (R)-[[(1-methyl-5-hexenyl)oxy]methyl]-benzene 
• 944797-05-1 (7R)-1-[(1'S,3a'S,6'R,7a'S)-1'-(1,1-dimethylethoxy)octahydro-7'a-methylspiro[1,3-dioxolane-2,5'-[5H]inden]-6'-yl]-7-(phenylmethoxy)-3-octanone 

Downstream Products

• 944797-07-3 (1S,3aS,8aR,9aS)-1-(1,1-dimethylethoxy)-1,2,3,3a,4,7,8,8a,9,9a-decahydro-9a-methyl-5-[(3R)-3-(phenylmethoxy)butyl]-6H-benz[f]inden-6-one 

Relevant academic research and scientific papers

Palladium-catalyzed potassium enoxyborate alkylation of enantiopure Hajos-Parrish indenone to construct rearranged steroid ring systems

(Chemical Equation Presented) Here we report the stereo- and regiospecific C-6 alkylation of a trans-inden-5-one (from optically pure Hajos-Parrish ketone) with allylic electrophiles. Use of this alkylation procedure has led to an improved synthesis of th