857283-26-2

Upstream product

• 857283-25-1 (2-benzyloxy-6-bromo-3-(1,3-dioxan-2-yl)-5-methoxy-4-methylphenyl)methanol 
• 857283-24-0 3-bromo-6-(1,3-dioxan-2-yl)-2-hydroxymethyl-4-methoxy-5-methylphenol 
• 1026631-04-8 4-bromo-2-hydroxy-3-hydroxymethyl-5-methoxy-6-methylbenzaldehyde 
• 808750-28-9 5-bromo-6-methoxy-2,2,7-trimethyl-4H-benzo[1,3]dioxin-8-carbaldehyde 

Downstream Products

• 857283-28-4 2-{(2-benzyloxy-4-bromo-5-methoxy)-(3RS)-[methoxy-(2-methoxy-6-vinylphenyl)methyl]-6-methylphenyl}-1,3-dioxane 
• 857283-23-9 2-benzyloxy-4-bromo-5-methoxy-3-[methoxy-(2-methoxy-6-vinyl-phenyl)-methyl]-6-methyl-benzaldehyde 
• 857283-27-3 {2-benzyloxy-6-bromo-3-(1,3-dioxan-2-yl)-5-methoxy-4-methylphenyl}-(2-methoxy-6-vinylphenyl)methanol 

Relevant academic research and scientific papers

Intramolecular Heck reactions for the synthesis of the novel antibiotic mensacarcin: Investigation of catalytic, electronic and conjugative effects in the preparation of the hexahydroanthracene core

The intramolecular Heck reaction of the three complex diphenyl substrates rac-2, 5 and rac-6, containing substituents with different electronic and conjugative properties, were examined. The Pd compounds [Pd2(dba) 3]/[(tBu)3/su