934749-90-3

Upstream product

• 53560-25-1 methyl 3-(3,4,5-trimethoxyphenyl)propionate 
• 25173-72-2 3-(3,4,5-trimethoxyphenyl)propanoic acid 
• 934749-87-8 3-(2-formyl-3,4,5-trimethoxy-phenyl)-propionic acid methyl ester 
• 934749-99-2 1-but-3-enyl-2-[1-(tert-butyl-dimethyl-silanyloxy)-3-trimethylsilanyl-prop-2-ynyl]-3,4,5-trimethoxy-benzene 
• 934749-88-9 3-{2-[1-(tert-butyl-dimethyl-silanyloxy)-3-trimethylsilanyl-prop-2-ynyl]-3,4,5-trimethoxy-phenyl}-propionic acid methyl ester 
• 934749-98-1 3-{2-[1-(tert-butyl-dimethyl-silanyloxy)-3-trimethylsilanyl-prop-2-ynyl]-3,4,5-trimethoxy-phenyl}-propan-1-ol 
• 934749-89-0 3-{2-[1-(tert-butyl-dimethyl-silanyloxy)-3-trimethylsilanyl-prop-2-ynyl]-3,4,5-trimethoxy-phenyl}-propionaldehyde 
• 934749-97-0 3-[2-(1-hydroxy-3-trimethylsilanyl-prop-2-ynyl)-3,4,5-trimethoxy-phenyl]-propionic acid methyl ester 

Downstream Products

• 1036001-13-4 C₁₆H₂₀O₄ 

Relevant academic research and scientific papers

Synthesis of new allocolchicinoids with seven- and eight-membered B-rings by enyne ring-closing metathesis

Total syntheses of allocolchicines 4 and 5, with the ester functionality in the C-ring at the C10 or C11 positions, is reported. An asymmetric synthesis of (7S)-allocolchicine 5 is also described. The main features included the elaboration of a common int

Synthesis of allocolchicines using sequential ring-closing enyne metathesis - Diels - Alder reactions

New allocolchinoids having functionality in the C ring at position C10 or C11 have been synthesized using the enyne ring-closing metathesis (RCM) reaction for construction of the seven-membered ring and a Diels-Alder-aromatization sequence for the elabora