612090-72-9

Upstream product

• 67-56-1 methanol 
• 201230-82-2 carbon monoxide 
• 612090-71-8 (Z)-1-((3-iodobut-2-enyloxy)methyl)-4-methoxybenzene 
• 89238-99-3 O-(4-methoxybenzyl)-trichloroacetimidate 

Downstream Products

• 612090-73-0 (2Z)-2-methyl-4-(4-methoxybenzyloxy)-2-buten-1-ol 
• 612090-74-1 (2Z)-4-(4-methoxybenzyloxy)-2-methyl-2-butenal 
• 880462-69-1 ethyl (4Z)-6-(4-methoxybenzyloxy)-2,2,4-trimethyl-3-triethylsiloxy-4-hexenoate 
• 880462-70-4 ethyl (4Z)-6-(4-methoxybenzyloxy)-4-methyl-3-triethylsiloxy-4-hexenoate 
• 1026000-99-6 (Z)-3-Hydroxy-6-(4-methoxy-benzyloxy)-2,2,4-trimethyl-hex-4-enoic acid ethyl ester 

Relevant academic research and scientific papers

Diastereoselective Palladium-Catalyzed Formate Reduction of Allylic Carbonates as a New Entry into Propionate Units

(Equation presented) The diastereoselective palladium-catalyzed formate reduction of allylic carbonates is described. Reduction of allylic carbonates under mild conditions (Pd(OAc)2 (2.5-5 mol %), [n-Bu 3PH]BF4 (2.5-5 mol

Diastereoselective palladium-catalyzed formate reduction of allylic carbonates en route to polypropionate systems

Diastereoselective palladium-catalyzed formate reduction of allylic carbonates presents unique opportunities for applications in target-oriented organic synthesis provided that selectivity, in particular stereoselectivity, in the course of this metal-cata