15402-82-1

Upstream product

• 128638-55-1 3,5-dimethoxy-β-methyl-β-nitrostyrene 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 18917-76-5 1,3-dimethoxy-5-(2-nitroprop-1-en-1-yl)benzene 

Downstream Products

• 128638-62-0 N-[2-(3,5-Dimethoxy-phenyl)-1-methyl-ethyl]-acetamide 
• 289889-81-2 (+/-)-N-trifluoroacetyl-1-[3,5-dimethoxy-4-(1-oxo-3-phenylpropy)phenyl]-2-aminopropane 
• 289889-88-9 (+/-)-N-trifluoroacetyl-1-[3,5-dimethoxy-4-(3-phenylpropyl)phenyl]-2-amionopropane 
• 289889-89-0 (+/-)-N-trifluoroacetyl-1-(3,5-dimethoxyphenyl)-2-aminopropane 

Relevant academic research and scientific papers

Novel dihydroquinolizinones for the treatment and prophylaxis of hepatitis B virus infection

The invention provides novel compounds having the general formula: wherein R1, R2, R3, R4, R5 and R6 are as described herein, compositions including the compounds and methods of using the compounds.

NOVEL DIHYDROQUINOLIZINONES FOR THE TREATMENT AND PROPHYLAXIS OF HEPATITIS B VIRUS INFECTION

The invention provides novel compounds having the general formula (I) wherein R1, R2 R3, R4, R5 and R6 are as described herein, compositions including the compounds and methods of using the compounds in the treatment of the hepatitis B virus.

The Stereoisomers of 5-Bromo-6,8-dimethoxy-1,2,3-trimethyl-1,2,3,4-tetrahydroisoquinoline: X-Ray Crystal Structure of the trans Isomer

Henry reaction between 3,5-dimethoxybenzaldehyde (2) and nitroethane gave (E)-2-(3,5-dimethoxyphenyl)-1-methyl-1-nitroethene (3).Under mild conditions the erythro and threo nitro aldols intermediate in this reaction could be isolated as their acetates.The