39508-15-1

Upstream product

• 917-64-6 methyl magnesium iodide 
• 2150-37-0 methyl 3,5-dimethoxybenzoate 
• 129918-78-1 N-<<1-(3,5-dimethoxyphenyl)-1-methylethoxy>carbonyl>cyclohexylamine 
• 39508-04-8 Ddz-L-Ala-OH 
• 39151-19-4 1-(3,5-dimethoxyphenyl)ethan-1-one 
• 557-93-7 2-bromoprop-1-ene 
• 20469-65-2 1-bromo-3,5-dimethoxybenzene 
• 1132-21-4 3,5-dimethoxybenzoic acid 
• 39508-01-5 (3’,5’-dimethoxy-1,1-dimethylbenzyloxy)carbonyl azide 
• 39508-00-4 3,5-dimethoxy-α,α-dimethylbenzylcarbazate 
• 39507-96-5 3,5-dimethoxy-α,α-dimethyl benzyl alcohol 
• 17275-82-0 ethyl 3,5-dimethoxybenzoate 

Downstream Products

• 34993-66-3 3,5-dihydroxy-1-isopropylbenzene 

Relevant academic research and scientific papers

Magnesiation of electron-rich aryl bromides and their use in nickel-catalyzed cross-coupling reactions

Electron-rich aryl bromides are rapidly converted to the corresponding lithium triarylmagnesiates with (n-Bu)3MgLi, which undergo efficient nickel-catalyzed Kumada-Corriu cross-coupling reactions with a variety of aryl and alkenyl bromides, chlorides, tosylates, and triflates.

Pinacolboratamethyl-enetriphenylphosphonium iodide, a new methylene transfer reagent

The title compound is easily prepared and reacts with various aldehydes and ketone. The reagent is compatible with free hydroxy groups. Yields with various aldehydes and ketones are in 50- > 99% range. Both aliphatic, aromatic and unsaturated carbonyls react.