162544-53-8

Upstream product

• 133332-31-7 (E)-3-(3-cyclopentyloxy-4-methoxyphenyl)-2-propenoic acid 
• 133332-20-4 (E)-methyl-3-<3-(cyclopenyloxy)-4-methoxyphenyl>prop-2-enoate 
• 137-43-9 Cyclopentyl bromide 
• 621-59-0 isovanillin 
• 67387-76-2 3-cyclopentyloxy-4-methoxybenzylaldehyde 

Downstream Products

• 194737-48-9 (2R)-2-(N-(E)-3-cyclopentyloxy-4-methoxycinnamoyl)amino-2-phenylethanol 
• 479258-10-1 (E)-1-[3-(3-cyclopentyloxy-4-methoxyphenyl)-2-propenoyl]-3,5-dimethyl-pyrazole 
• 194737-50-3 (R)-2-(3-Cyclopentyloxy-4-methoxy-phenyl)-3-((R)-4-phenyl-4,5-dihydro-oxazol-2-yl)-propionitrile 
• 194737-52-5 (2R,4R)-2-[4-(3-cyclopentyloxy-4-methoxyphenyl)pyrrolin-2-yl]amino-2-phenylethanol 
• 194737-49-0 (4R)-2-(E)-[2-(3-cyclopentyloxy-4-methoxyphenyl)ethenyl]-4-phenyl-4,5-dihydroxyoxazole 
• 85416-75-7 (R)-4-(3-cyclopentyloxy-4-methoxyphenyl)pyrrolidin-2-one 
• 479258-11-2 3,5-dimethyl-1-[4-nitro-3-(3-cyclopentyloxy-4-methoxyphenyl)butanoyl]pyrazole 

Relevant academic research and scientific papers

Enantioselective Michael additions of nitromethane by a catalytic double activation method using chiral Lewis acid and achiral amine catalysts

Reactions of nitromethane with 1-(2-alkenoyl)-3,5-dimethylpyrazoles can be effectively catalyzed by R,R-DBFOX/Ph·Ni(ClO4)2·3H2O and achiral amine bases, each in a catalytic loading of 10 mol %, to give 1-(3-substituted 4-n

Synthesis of the novel antidepressant (R)-(-)-Rolipram

Enantioselective synthesis of (R)-Rolipram 1 has been achieved through a conjugate addition of cyanide to enantiomerically pure 2-(2-aryl ethenyl)oxazoline 2, followed by selective reduction of the adduct with NaBH4-NiCl2.