1333320-16-3

Upstream product

• 105-13-5 4-Methoxybenzyl alcohol 
• 89238-99-3 O-(4-methoxybenzyl)-trichloroacetimidate 
• 5407-87-4 2-Amino-4,6-dimethylpyridine 
• 5006-58-6 2,3,5-tribromo-4,6-dimethylpyridine 
• 4039-83-2 3-(4-methoxybenzyloxy)propyne 
• 5407-86-3 3,5-dibromo-4,6-dimethylpyridin-2-amine 

Downstream Products

• 1333320-19-6 2-(3-(4-methoxybenzyloxy)propyl)-3,5-dibromo-4,6-dimethylpyridine 
• 1333320-21-0 3-(3,5-di((Z)-dec-1-enyl)-4,6-dimethylpyridin-2-yl)propan-1-ol hydrochloride 
• 1333320-23-2 3-(4,6-dimethyl-3,5-di((E)-prop-1-enyl)pyridin-2-yl)propan-1-ol hydrochloride 
• 1333320-24-3 2-(3-(4-methoxybenzyloxy)propyl)-5-bromo-3-((E)-dec-1-enyl)-4,6-dimethylpyridine 
• 1333320-25-4 2-(3-(4-methoxybenzyloxy)propyl)-3-bromo-5-((E)-dec-1-enyl)-4,6-dimethylpyridine 
• 1333320-27-6 3-(3-((E)-dec-1-enyl)-5-((Z)-dec-1-enyl)-4,6-dimethylpyridin-2-yl)propan-1-ol hydrochloride 
• 1333320-29-8 3-(5-((E)-dec-1-enyl)-3-((Z)-dec-1-enyl)-4,6-dimethylpyridin-2-yl)propan-1-ol hydrochloride 

Relevant academic research and scientific papers

Regio- and stereoselective syntheses of the natural product CCR5 antagonist anibamine and its three olefin isomers

The syntheses of the natural product anibamine and its three olefin isomers have been achieved concisely and efficiently via highly regio- and stereoselective reactions. The crucial steps included a regioselective palladium-catalyzed alkynylation by Sonogashira coupling and a stereoselective Suzuki coupling. Further conformation analyses and in vitro calcium mobilization studies were carried out to characterize the compounds' biological properties.