886450-89-1

Upstream product

• 271578-70-2 4-[2-(tert-butyl-dimethyl-silanyloxymethyl)-3,4,6-trimethoxy-5-methyl-phenyl]-but-2-en-1-ol 
• 24424-99-5 di-tert-butyl dicarbonate 
• 886450-34-6 {1-(2,2-dimethyl-[1,3]dioxolan-4-yl)-2-[2,4,5-trimethoxy-6-(4-methoxy-benzyloxymethyl)-3-methyl-phenyl]-ethyl}-methyl-carbamic acid tert-butyl ester 
• 886450-33-5 {1-(2,2-dimethyl-[1,3]dioxolan-4-yl)-2-[2,4,5-trimethoxy-6-(4-methoxy-benzyloxymethyl)-3-methyl-phenyl]-ethyl}-carbamic acid tert-butyl ester 
• 886450-31-3 [2-[2-(tert-butyl-dimethyl-silanyloxymethyl)-3,4,6-trimethoxy-5-methyl-phenyl]-1-(2,2-dimethyl-[1,3]dioxolan-4-yl)-ethyl]-carbamic acid tert-butyl ester 
• 886450-30-2 {2-[2-azido-2-(2,2-dimethyl-[1,3]dioxolan-4-yl)-ethyl]-3,5,6-trimethoxy-4-methyl-benzyloxy}-tert-butyl-dimethyl-silane 
• 886450-32-4 [1-(2,2-dimethyl-[1,3]dioxolan-4-yl)-2-(2-hydroxymethyl-3,4,6-trimethoxy-5-methyl-phenyl)-ethyl]-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

The solution to a deep stereochemical conundrum: Studies toward the tetrahydroisoquinoline alkaloids

(Chemical Equation Presented) Facile construction of subunits 1 and 2 allowed the rapid assembly of the pentacyclic ring system 3 of the cytotoxic tetrahydroisoquinoline alkaloids. A surprising participation reaction was discovered, which necessitated rev