945006-77-9

Upstream product

• 945006-75-7 4-bromo-1-(4-methoxybenzyl)-2-methylsulfanyl-5-vinylimidazole 
• 945006-76-8 1-(4-methoxybenzyl)-2-methylsulfanyl-5-vinylimidazole-4-carboxylic acid 
• 593-56-6 N-methoxylamine hydrochloride 

Downstream Products

• 945006-78-0 4-chloro-1-(4-methoxy-benzyl)-2-methylsulfanyl-1H-imidazo[4,5-c]pyridine 
• 945006-64-4 1-(4-methoxybenzyl)-4-(1H-pyrrol-2-yl)-1H-imidazo[4,5-c]pyridine 
• 945006-79-1 2-[1-(4-methoxybenzyl)-1H-imidazo[4,5-c]pyridin-4-yl]pyrrole-1-carboxylic acid tert-butyl ester 
• 945006-68-8 2-[2-azido-1-(4-methoxybenzyl)-1H-imidazo[4,5-c]pyridin-4-yl]pyrrole-1-carboxylic acid tert-butyl ester 
• 945006-67-7 2-[2-methanesulfinyl-1-(4-methoxybenzyl)-1H-imidazo[4,5-c]pyridin-4-yl]pyrrole-1-carboxylic acid tert-butyl ester 
• 945006-63-3 2-[1-(4-methoxybenzyl)-2-methylsulfanyl-1H-imidazo[4,5-c]pyridin-4-yl]pyrrole-1-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

Application of a 6π-1-azatriene electrocyclization strategy to the total synthesis of the marine sponge metabolite ageladine A and biological evaluation of synthetic analogues

(Chemical Equation Presented) A 12-step synthesis of the angiogenesis inhibitory marine metabolite ageladine A is reported. The key steps include a 6π-1-azatriene electrocyclization for formation of the pyridine ring and a Suzuki-Miyaura coupling of N-Boc