142501-56-2

Upstream product

• 142501-54-0 (1RS,2RS,3SR)-4-(4-hydroxy-3,5-dimethoxyphenyl)-2,3-dimethyl-1-(3,4,5-trimethoxyphenyl)butyl acetate 
• 142501-53-9 (1RS,2RS,3SR)-4-(4-benzyloxy-3,5-dimethoxyphenyl)-2,3-dimethyl-1-(3,4,5-trimethoxyphenyl)butyl acetate 
• 142501-51-7 (2RS,3SR)-4-(4-benzyloxy-3,5-dimethoxyphenyl)-2,3-dimethyl-1-(3,4,5-trimethoxyphenyl)butan-1-one 
• 142501-45-9 (2R,3S)-4-(4-Benzyloxy-3,5-dimethoxy-phenyl)-2,3-dimethyl-1-(3,4,5-trimethoxy-phenyl)-butan-1-ol 
• 142501-50-6 4-(4-benzyloxy-3,5-dimethoxyphenyl)-3-methyl-1-(3,4,5-trimethoxyphenyl)butan-1-one 
• 138566-51-5 3-(4-benzyloxy-3,5-dimethoxyphenyl)-2-methylpropyl p-toluenosulfonate 
• 142501-48-2 (3,4,5-trimethoxyphenyl)(trimethylsilyloxy)acetonitrile 

Downstream Products

• 142501-46-0 (1α,2α,3β,4α)-4-(3,4-dihydroxy-5-methoxyphenyl)-5,6,7-trimethoxy-2,3-dimethyl-1,2,3,4-tetrahydronaphthalen-1-yl acetate 

Relevant academic research and scientific papers

Intramolecular Oxidative Coupling of Aromatic Compounds. III. Monophenolic Substrates

The synthesis of (2RS,3SR)-4-(4-hydroxy-3,5-dimethoxyphenyl)-2,3-dimethyl-1-(3,4,5-trimethoxyphenyl)butan-1-one (9) is described.Monophenolic oxidative coupling of (9) did not give any useful result.Oxidation of the derived acetoxy compound (18) by chemic