866110-60-3

Upstream product

• 866110-59-0 (3S,5S,6R)-3-[5-(tert-Butyl-dimethyl-silanyloxy)-2,4-dimethoxy-3-methyl-benzyl]-5,6-diphenyl-morpholin-2-one 
• 50-00-0 formaldehyd 
• 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 
• 866110-56-7 1-Benzyloxy-5-iodomethyl-2,4-dimethoxy-3-methyl-benzene 

Downstream Products

• 866110-68-1 C₆₀H₈₄N₂O₁₁Si₂ 
• 866110-82-9 {2-(8-allyloxy-1-allyloxymethyl-3-hydroxymethyl-5,7-dimethoxy-6-methyl-3,4-dihydro-1H-isoquinolin-2-yl)-1-[5-(tert-butyl-dimethyl-silanyloxy)-2,4-dimethoxy-3-methyl-benzyl]-2-oxo-ethyl}-methyl-carbamic acid 9H-fluoren-9-ylmethyl ester 
• 866110-69-2 {2-(8-allyloxy-1-allyloxymethyl-3-formyl-5,7-dimethoxy-6-methyl-3,4-dihydro-1H-isoquinolin-2-yl)-1-[5-(tert-butyl-dimethyl-silanyloxy)-2,4-dimethoxy-3-methyl-benzyl]-2-oxo-ethyl}-methyl-carbamic acid 9H-fluoren-9-ylmethyl ester 
• 866110-61-4 3-[5-(tert-butyl-dimethyl-silanyloxy)-2,4-dimethoxy-3-methyl-phenyl]-2-[(9H-fluoren-9-ylmethoxycarbonyl)-methyl-amino]-propionic acid 

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