18776-18-6

Upstream product

• 2806-85-1 3-ethoxypropanal 
• 100-42-5 styrene 
• 64-17-5 ethanol 
• 4393-06-0 1-Phenyl-2-propen-1-ol 
• 100-52-7 benzaldehyde 
• 133270-77-6 3-(tert-Butyl-dimethyl-silanyloxy)-3-ethoxy-1-phenyl-propan-1-ol 
• 24491-59-6 3-Chlor-3-phenyl-propyl-ethylether 

Downstream Products

• 137040-15-4 4-Ethoxy-2-hydroxy-2-phenyl-butyric acid 1-aza-bicyclo[2.2.2]oct-3-yl ester 
• 137039-87-3 4-Ethoxy-2-phenyl-2-trimethylsilanyloxy-butyronitrile 
• 137040-08-5 4-Ethoxy-2-hydroxy-2-phenyl-butyric acid ethyl ester 
• 137039-94-2 4-Ethoxy-2-hydroxy-2-phenyl-butyramide 
• 137040-01-8 4-Ethoxy-2-hydroxy-2-phenyl-butyric acid 
• 34008-71-4 3-ethoxy-1-phenyl-1-propanone 

Relevant academic research and scientific papers

A formal anti-Markovnikov hydroalkoxylation of allylic alcohols with a ruthenium catalyst

Hydroalkoxylation of C-C double bonds was achieved through the use of a ruthenium catalyst. The reaction of allylic alcohols with nucleophilic alcohols was carried out in the presence of a ruthenium catalyst prepared by RuClH(CO)(PPh3)3 and 2,6-bis(n-butyliminomethyl)-4-(piperidin-1-yl)pyridine under mild reaction conditions to afford the corresponding γ-alkoxypropanols in good yield.

Synthesis and Muscarinic Cholinergic Receptor Affinities of 3-Quinuclidinyl α-(Alkoxyalkyl)-α-aryl-α-hydroxyacetates

Seven analogues of 3-quinuclidinyl benzilate (QNB) in which one phenyl ring was replaced by an alkoxyalkyl moiety were synthesized and their affinities for the muscarinic cholinergic receptor determined.An oxygen in the β-position of the moienty was not w

Enantioselective Chiral Borane-Mediated Aldol Reactions of Silyl Ketene Acetals with Aldehydes. Novel Effect of the Trialkylsilyl Group of the Silyl Ketene Acetal on the Reaction Course

Highly enantioselective aldol reactions of silyl ketene acetals with a variety of aldehydes were achieved by using chiral boranes prepared from the sulfonamides of α-amino acids.