866110-63-6

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 866110-56-7 1-Benzyloxy-5-iodomethyl-2,4-dimethoxy-3-methyl-benzene 
• 866110-62-5 ((R)-1,2-Diphenyl-ethyl)-[(S)-2-(5-hydroxy-2,4-dimethoxy-3-methyl-phenyl)-1-hydroxymethyl-ethyl]-carbamic acid tert-butyl ester 
• 866110-57-8 (3S,5S,6R)-3-(5-Benzyloxy-2,4-dimethoxy-3-methyl-benzyl)-2-oxo-5,6-diphenyl-morpholine-4-carboxylic acid tert-butyl ester 

Downstream Products

• 866110-64-7 (1S,3S)-3-(tert-Butyl-dimethyl-silanyloxymethyl)-2-((R)-1,2-diphenyl-ethyl)-8-hydroxy-5,7-dimethoxy-6-methyl-1,2,3,4-tetrahydro-isoquinoline-1-carboxylic acid ethyl ester 

Relevant academic research and scientific papers

Asymmetric total syntheses of (-)-jorumycin, (-)-renieramycin G, 3-epi-jorumycin, and 3-epi-renieramycin G

The total synthesis of (-)-jorumycin (1) and (-)-renieramycin G (2) has been accomplished in 25 and 23 steps, respectively, from 5-benzyloxy-2,4- dimethoxy-3-methyl-benzyl alcohol. The synthesis features a substrate-tunable stereoselective intramolecular