656240-50-5

Upstream product

• 183803-06-7 3-hydroxy-4-methyliodobenzene 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 656240-46-9 (3R,5S)-5-(2-Bromo-5-methoxymethoxy-4-methyl-phenyl)-7-(tert-butyl-diphenyl-silanyloxy)-2-methyl-heptane-2,3-diol 
• 656240-47-0 2-{(2R,4S)-4-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-6-methoxymethoxy-7-methyl-chroman-2-yl}-propan-2-ol 
• 656240-45-8 (3R,5S)-7-(tert-Butyl-diphenyl-silanyloxy)-5-(3-methoxymethoxy-4-methyl-phenyl)-2-methyl-heptane-2,3-diol 
• 656240-52-7 acetic acid 5-(tert-butyl-diphenyl-silanyloxy)-3-(3-methoxymethoxy-4-methyl-phenyl)-pentyl ester 
• 656240-42-5 5-(tert-butyl-diphenyl-silanyloxy)-3-(3-methoxymethoxy-4-methyl-phenyl)-pentanoic acid 
• 656240-44-7 tert-butyl-[3-(3-methoxymethoxy-4-methyl-phenyl)-6-methyl-hept-5-enyloxy]-diphenyl-silane 
• 656240-40-3 5-(tert-butyl-diphenyl-silanyloxy)-3-(3-methoxymethoxy-4-methyl-phenyl)-pentan-1-ol 
• 656240-41-4 5-(tert-butyl-diphenyl-silanyloxy)-3-(3-methoxymethoxy-4-methyl-phenyl)-pentanal 
• 1027052-37-4 acetic acid 5-acetoxy-3-(3-methoxymethoxy-4-methyl-phenyl)-pentyl ester 
• 656240-39-0 Acetic acid (S)-5-hydroxy-3-(3-methoxymethoxy-4-methyl-phenyl)-pentyl ester 
• 656240-38-9 3-(3-methoxymethoxy-4-methyl-phenyl)-pentane-1,5-diol 
• 656240-37-8 3-(3-methoxymethoxy-4-methyl-phenyl)-pent-4-en-1-ol 

Relevant academic research and scientific papers

Substituted thieno[3,2-C]pyridine carboxylic acid derivatives

There are provided compounds of the formula wherein R1, R2, R3, X, ring A and ring B are as described. The compounds exhibit anticancer properties.

An Alternative Total Synthesis of (-)-Heliannuol E1

An efficient, enantiocontrolled total synthesis of (-)-heliannuol E has been accomplished using a palladium-catalyzed cyclization of the six-membered oxygen containing heterocycle as the key reaction step.