113296-71-2

Upstream product

• 560115-31-3 (2-benzyloxy-3,5-dimethoxy-4-methylphenyl)methanol 
• 100-39-0 benzyl bromide 
• 85071-58-5 2-hydroxy-3,5-dimethoxy-4-methylbenzaldehyde 

Downstream Products

• 1054608-39-7 (2S,5R,6R)-methyl-6-(2-(benzyloxy)-3,5-dimethoxy-4-methylphenyl)-3,5-dimethyl-5,6-dihydro-2H-pyran-2-carboxylate 
• 113296-84-7 3-[1-(2-Benzyloxy-3,5-dimethoxy-4-methyl-phenyl)-meth-(Z)-ylidene]-6-(2,4,5-trimethoxy-3-methyl-benzyl)-piperazine-2,5-dione 
• 654077-35-7 N-(2-benzyloxy-3,5-dimethoxy-4-methylbenzyl)-2,2-dimethoxy-N-tosylethylamine 
• 654077-45-9 1-benzoylaminomethyl-8-hydroxy-5,7-dimethoxy-6-methylisoquinoline 
• 654077-34-6 N-(2-benzyloxy-3,5-dimethoxy-4-methylbenzyl)-2,2-dimethoxyethylamine 
• 654077-40-4 8-benzoyloxy-1-cyano-5,7-dimethoxy-6-methylisoquinoline 
• 654077-37-9 8-benzyloxy-1-cyano-5,7-dimethoxy-6-methylisoquinoline 
• 654077-36-8 8-benzyloxy-5,7-dimethoxy-6-methylisoquinoline 
• 113296-79-0 (Z)-1-acetyl-3-(2-benzyloxy-3,5-dimethoxy-4-methylphenylmethylene)-6-(2,4,5-trimethoxy-3-methylphenylmethyl)-2,5-piperazinedione 

Relevant academic research and scientific papers

Total synthesis of (-)-kendomycin

(Chemical Equation Presented) An enantioselective synthesis of (-)-kendomycin is described and is based on the application of the organosilane-based [4 + 2]-annulation strategy for the assembly of the C1a-C10 fragment. An underutilized samarium(II) iodide

Catalytic hydrogenation of 8-acyloxy-1-cyanoiso-quinoline and synthesis of 9-methoxy-9-deethoxy-cribrostatin 6

Catalytic hydrogenation of 8-acyloxy-1-cyanoisoquinolines (6) ～(9) in the presence of 10% Pd-C and synthesis of 9-methoxy isomer (10) of cribrostatin 6 utilizing the compound (26) obtained by this reaction are described.