1008303-69-2

Upstream product

• 1008303-68-1 C₂₁H₂₁ClO₆ 
• 122775-35-3 3,4-Dimethoxyphenylboronic acid 
• 77784-64-6 Naphtho<2,3-d>-1,3-dioxole-5-ol 
• 1008303-67-0 (1R,3R)-3-(3,4-dimethoxyphenyl)-4,4-ethylenedioxy-1-hydroxy-6,7-methylenedioxy-1,2,3,4-tetrahydronaphthalene 
• 1008303-61-4 (R)-3-(3,4-dimethoxyphenyl)-4,4-ethylenedioxy-6,7-methylenedioxy-1-oxo-1,2,3,4-tetrahydronaphthalene 
• 1008303-50-1 4,4-ethylenedioxy-6,7-methylenedioxy-1-oxo-1,4-dihydronaphthalene 

Downstream Products

• 41303-46-2 (R)-2-(3,4-dimethoxyphenyl)-6,7-methylenedioxy-1-oxo-1,2,3,4-tetrahydronaphthalene 

Relevant academic research and scientific papers

Asymmetric 1,4-addition of organoboron reagents to quinone monoketals catalyzed by a chiral diene/rhodium complex: A new synthetic route to enantioenriched 2-aryltetralones

A novel synthetic approach to 2-aryltetra-lones with high ee has been developed through asymmetric 1,4-addition of arylboronic acids to naphthoquinone monoketals catalyzed by a rhodium complex with the (R,R)-Ph-bod* ligand. The asymmetric addition proceed