101615-10-5

Upstream product

• 20933-24-8 2-bromo-6-methoxy-1-tetralone 
• 352-13-6 4-flourophenylmagnesium bromide 
• 1078-19-9 6-methoxy-3,4-dihydro-1(2H)-naphthalenone 
• 79-37-8 oxalyl dichloride 
• 40759-46-4 1-(2-methanesulfonyloxyethyl)-3-methoxybenzene 
• 101615-08-1 2-p-fluorophenyl-4-m-methoxyphenylbutyric acid 
• 405-50-5 p-Fluorophenylacetic acid 
• 352-33-0 1-Chloro-4-fluorobenzene 
• 190972-21-5 2-(4-Fluoro-phenyl)-4-(3-methoxy-phenyl)-butyronitrile 
• 2146-61-4 3-methoxyphenethyl bromide 

Relevant academic research and scientific papers

N-heterocyclic carbene-palladium(II)-1-methylimidazole complex catalyzed α-arylation reactions of tetralones with aryl chlorides and further transformation of the products

NHC-Pd(II)-Im complex 1 has proven to be an efficient catalyst in the reaction between tetralones 2 and aryl chlorides 3, giving the α-arylated tetralones 4 in good to high yields. In addition, if the above reaction mixture was exposed to air at room temp

Aryltricyclospirodienones; novel steroid mimics as inhibitors of aromatase

The aryltricyclospirodienones 16a, 16b, 16c and 18 have been designed as potential inhibitors of aromatase and are synthesised from 6-methoxytetralone; ? compounds 16a and 18 have proved effective inhibitors with activities of the same order as aminoglutethimide.

Phenol derivatives

A phenol derivative of the formulaNU--A--X--R 1wherein NU is a defined phenolic nucleus including a phenyl-hydroxynaphthyl; hydroxyphenyl-naphthyl; phenyl-hydroxyindanyl, phenyl-hydroxybenzothienyl or mono-hydroxyphenyl-ethylene or vinylene nucleus; where