171013-46-0

Upstream product

• 7149-92-0 2,4-dimethoxy-3-methylbenzaldehyde 
• 50-00-0 formaldehyd 
• 19676-67-6 2,4-dimethoxy-3-methylphenol 

Downstream Products

• 171013-47-1 2,3,5-trimethoxy-4-methylbenzyl alcohol 
• 271578-78-0 1,3,4-trimethoxy-2-methyl-5-vinylbenzene 
• 398143-07-2 (R)-2-Benzyloxy-1-(2,3,5-trimethoxy-4-methyl-phenyl)-ethylamine 
• 271578-85-9 (R)-1-Benzyloxymethyl-5,7,8-trimethoxy-6-methyl-1,2,3,4-tetrahydro-isoquinolin-4-ol 
• 271578-83-7 [2-benzyloxy-1-(2,3,5-trimethoxy-4-methyl-phenyl)-ethyl]-carbamic acid tert-butyl ester 
• 271578-84-8 [(R)-2-Benzyloxy-1-(2,3,5-trimethoxy-4-methyl-phenyl)-ethyl]-(2,2-diethoxy-ethyl)-amine 
• 398142-93-3 1-benzyloxymethyl-4-hydroxy-5,7,8-trimethoxy-6-methyl-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester 
• 171013-38-0 (2-Iodo-3,5,6-trimethoxy-4-methyl-phenyl)-acetic acid methyl ester 
• 171013-48-2 2-Iodo-3,5,6-trimethoxy-4-methyl-benzaldehyde 
• 171013-37-9 (2-Iodo-3,5,6-trimethoxy-4-methyl-phenyl)-methanol 
• 560115-36-8 8-benzyloxy-3-benzyloxymethyl-5,7-dimethoxy-6-methyl-1-phenylsulfanylmethyl-1H-isoquinoline-2-carboxylic acid methyl ester 
• 560115-35-7 8-benzyloxy-3-benzyloxymethyl-5,7-dimethoxy-6-methylisoquinoline 

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

New strategy for the synthesis of tetrahydroisoquinoline alkaloids

(Matrix presented) A general strategy for the formation of 1,3-cis-substituted tetrahydroisoquinolines is described from ortho-iodo imines involving Larock isoquinoline synthesis, addition of organolithium compounds to unactivated isoquinolines, and ionic