80314-60-9

Upstream product

• 80314-64-3 2-(chloromethyl)-1-methoxy-4-(2-methoxyethyl)benzene 
• 80314-58-5 1-methoxy-4-(2-methoxyethyl)benzene 
• 702-23-8 2-(4-Methoxyphenyl)ethanol 
• 104-01-8 4-Methoxyphenylacetic acid 
• 80314-59-6 <2'-methoxy-5'-(2''-methoxyethyl)phenyl>acetonitrile 
• 141-78-6 ethyl acetate 

Downstream Products

• 80318-67-8 dimethyl 3,6,8-trihydroxy-7-<2'-methoxy-5'-(2''-methoxyethyl)phenyl>-9,10-dioxo-9,10-dihydroanthracene-1,2-dicarboxylate 
• 80314-57-4 1-Methoxy-4-(2-methoxy-ethyl)-2-{1-[1-methoxy-1-trimethylsilanyloxy-meth-(Z)-ylidene]-2-trimethylsilanyloxy-allyl}-benzene 
• 80314-62-1 (E)-2-[2-Methoxy-5-(2-methoxy-ethyl)-phenyl]-3-trimethylsilanyloxy-but-2-enoic acid methyl ester 

Relevant academic research and scientific papers

Chemistry of the Coccoidea. X Synthesis of the Xantholaccaic Acid B System and of Related Compounds

Xantholaccaic acid B dimethyl ester pentamethyl ether (6) and some related anthraquinones have been synthesized by regiospecific Diels-Alder addition of the highly functionalized dienes (12) and (27) successively to 2,6-dichloro-1,4-benzoquinone.This is the first synthesis of the β-arylanthraquinone skeleton characteristic of the water-soluble dyestuffs from lac insects.

SYNTHESIS OF THE XANTHOLACCAIC ACID B SYSTEM

The xantholaccaic acid B system has been synthesized for the first time by successive regiospecific Diels-Alder reactions.