94236-22-3

Upstream product

• 3970-21-6 2-Methoxyethoxymethyl chloride 
• 95-56-7 2-hydroxybromobenzene 

Downstream Products

• 205505-80-2 [(S)-2,2-Dimethyl-4-(3,4,5-trimethoxy-benzyl)-[1,3]dioxolan-4-yl]-[2-(2-methoxy-ethoxymethoxy)-phenyl]-methanone 
• 205505-78-8 [(S)-4-(3,4-Dimethoxy-benzyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-[2-(2-methoxy-ethoxymethoxy)-phenyl]-methanone 
• 205505-75-5 [(S)-4-(4-Methoxy-benzyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-[2-(2-methoxy-ethoxymethoxy)-phenyl]-methanone 
• 205505-76-6 [(S)-4-(3-Methoxy-benzyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-[2-(2-methoxy-ethoxymethoxy)-phenyl]-methanone 
• 205505-41-5 ((S)-4-Benzyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-[2-(2-methoxy-ethoxymethoxy)-phenyl]-methanone 
• 167165-56-2 3-bromo-2-(2-methoxyethoxymethoxy)benzaldehyde 

Relevant academic research and scientific papers

Modular P-chirogenic aminophosphane-phosphinite ligands for Rh-catalyzed asymmetric hydrogenation: A new model for prediction of enantioselectivity

An original series of P-chirogenic aminophosphane-phosphinite (AMPP) ligands has been synthesized from (+)- or (-)-ephedrine in 23 to 61 % overall yields by a versatile three-step methodology. The AMPP ligands, bearing either one or two P-chirogenic cente

A new chiral multidentate ligand for asymmetric catalysis

The synthesis of enantiomerically pure (R,R)-N,N'-bis(3-diphenylphosphino-2-hydroxybenzylidene)-1,2-diphenyl- 1,2-ethanediamine (1) is described. This multidentate salentype ligand offers several possibilities for the construction of chiral mono-nuclear o