137039-83-9

Upstream product

• 67-56-1 methanol 
• 22731-70-0 1-(4-bromophenyl)prop-2-en-1-one 
• 99-90-1 para-bromoacetophenone 
• 173019-84-6 1-bromo-4-(3-bromoprop-1-yn-1-yl)benzene 
• 1416983-92-0 C₉H₇BrO₂ 
• 137040-23-4 1-(4-Bromo-phenyl)-3-methoxy-propan-1-ol 
• 2039-82-9 1-bromo-4-ethenyl-benzene 
• 55440-96-5 1-Chlor-3-methoxy-1-(4-brom-phenyl)-propan 

Downstream Products

• 137039-89-5 2-(4-Bromo-phenyl)-4-methoxy-2-trimethylsilanyloxy-butyronitrile 
• 137040-17-6 2-(4-Bromo-phenyl)-2-hydroxy-4-methoxy-butyric acid 1-aza-bicyclo[2.2.2]oct-3-yl ester 
• 137040-10-9 2-(4-Bromo-phenyl)-2-hydroxy-4-methoxy-butyric acid ethyl ester 
• 137039-96-4 2-(4-Bromo-phenyl)-2-hydroxy-4-methoxy-butyramide 
• 137040-03-0 2-(4-Bromo-phenyl)-2-hydroxy-4-methoxy-butyric acid 

Relevant academic research and scientific papers

Oxa-Michael addition promoted by the aqueous sodium carbonate

An efficient Michael addition of alcohols to activated alkenes promoted by sodium carbonate with water as reaction medium has been developed. The reaction provides a general, economical and environmentally friendly approach for the synthesis of β-alkoxycarbonyl compounds.

Unveiling the reactivity of propargylic hydroperoxides under gold catalysis

Controlled gold-catalyzed reactions of primary and secondary propargylic hydroperoxides with a variety of nucleophiles including alcohols, phenols, 2-hydroxynaphthalene-1,4-dione, and indoles allow the direct and efficient synthesis of β-functionalized ke

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