860638-84-2

Upstream product

• 53560-33-1 3,4,5-trimethoxyphenylacetylene 
• 21900-52-7 5-bromo-2-chloro-benzoyl chloride 

Downstream Products

• 860638-83-1 (R)-methyl 4-chloro-3-(1-(methoxymethoxy)-3-(3,4,5-trimethoxyphenyl)propyl)benzoate 
• 860638-87-5 (R)-5-(3-(5-bromo-2-chlorophenyl)-3-(methoxymethoxy)propyl)-1,2,3-trimethoxybenzene 
• 860638-86-4 (S)-5-(3-(5-bromo-2-chlorophenyl)-3-(methoxymethoxy)prop-1-ynyl)-1,2,3-trimethoxybenzene 
• 860781-52-8 (S)-5-(3-(2-bromophenyl)-3-(methoxymethoxy)prop-1-ynyl)-1,2,3-trimethoxybenzene 
• 860638-90-0 (R)-5-(3-(2-bromophenyl)-3-(methoxymethoxy)propyl)-1,2,3-trimethoxybenzene 
• 860638-89-7 (S)-1-(2-bromophenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-yn-1-ol 
• 860638-85-3 (S)-1-(5-bromo-2-chlorophenyl)-3-(3,4,5-trimethoxyphenyl)prop-2-yn-1-ol 

Relevant academic research and scientific papers

Allocolchicinoid synthesis via direct arylation

(Chemical Equation Presented) A formal enantioselective synthesis of allocolchicine and a synthesis of a C-ring analogue have been achieved by employing an intramolecular direct arylation of an aryl chloride to form the biaryl carbon-carbon bond and the s