308804-94-6

Upstream product

• 211935-25-0 2-benzyloxy-3,6-dimethoxybenzaldehyde 
• 308804-89-9 Methyl 3-(4-chloromethylphenoxy)-4-methoxybenzoate 
• 64466-51-9 3,6-Dimethoxy-2-hydroxybenzaldehyde 
• 100-44-7 benzyl chloride 
• 135303-88-7 Methyl 3-(4-(hydroxymethyl)phenoxy)-4-methoxybenzoate 
• 135303-87-6 methyl 3-(4'-formylphenoxy)-4-methoxybenzoate 

Downstream Products

• 308804-97-9 Methyl 3-(4-{2-[3,6-dimethoxy-2-(3-methyloxycarbonyl-4-nitrophenoxy)phenyl]ethyl}phenoxy)-4-methoxybenzoate 
• 308804-98-0 Methyl 3-(4-{2-[2-(4-amino-3-methyloxycarbonylphenoxy)-3,6-dimethoxyphenyl]ethyl}phenoxy)-4-methoxybenzoate 
• 308805-00-7 Methyl 3-(4-{2-[3,6-dimethoxy-2-(3-methyloxycarbonylphenoxy)phenyl]ethyl}phenoxy)-4-methoxybenzoate 
• 308805-02-9 [3-(4-{2-[2-(3-Hydroxymethylphenoxy)-3,6-dimethoxyphenyl]ethyl}phenoxy)-4-methoxyphenyl]methanol 
• 308805-03-0 2-{2-[4-(5-Chloromethyl-2-methoxyphenoxy)phenyl]ethyl}-3-(3-chloromethylphenoxy)-1,4-dimethoxybenzene 
• 308804-96-8 Methyl 3-{4-[2-(2-hydroxy-3,6-dimethoxyphenyl)ethyl]phenoxy}-4-methoxybenzoate 

Relevant academic research and scientific papers

Solvent effect in the Wittig reaction under Boden's conditions

An interesting change in the stereochemical outcome of the Wittig olefination reaction under Boden's conditions (potassium bases and 18-crown-6 as the ylide forming reagent) is reported. This effect depends significantly on the polarity of the solvents an

Total synthesis of Marchantinquinone

The first synthesis of the title compound is described. Salient features include biaryl ether formation through S(N)Ar reactions and macrocyclization via a [Ni]0 mediated intramolecular coupling reaction.