21855-86-7

Upstream product

• 1220698-84-9 1-methoxy-4-(5-phenylpent-1-yn-1-yl)benzene 
• 826-73-3 1-Benzosuberone 
• 13139-86-1 4-methoxyphenyl magnesium bromide 

Downstream Products

• 1269617-57-3 C₁₈H₁₇ClO 
• 1269617-56-2 C₁₈H₁₇FO 
• 107388-28-3 ethyl α-methyl-α-propionate 
• 107388-30-7 Ethyl α-acetate 
• 107388-29-4 α-methyl-α-propionic acid 
• 107388-31-8 α-methyl-α-acetic acid 
• 107388-27-2 1-(p-Acetoxyphenyl)benzosuber-1-ene 
• 103304-52-5 6,7-dihydro-8-phenyl-9-{4-[2-(dimethylamino)ethoxy]phenyl}-5H-benzocycloheptene 
• 103304-55-8 6,7-dihydro-8-phenyl-9-(4-methoxyphenyl)-5H-benzocycloheptene 
• 103304-51-4 6,7-dihydro-8-phenyl-9-(4-hydroxyphenyl)-5H-benzocycloheptene 
• 103304-54-7 6,7-dihydro-8-bromo-9-(4-methoxyphenyl)-5H-benzocycloheptene 
• 107388-26-1 1-(p-Hydroxyphenyl)benzosuber-1-ene 

Relevant academic research and scientific papers

Cu-catalyzed intramolecular hydroarylation of alkynes

An efficient Cu-catalyzed intramolecular hydroarylation reaction of alkynes has been developed. The reaction is accomplished under mild conditions and shows good tolerance to both electron-rich and electron-deficient aryl nucleophiles. A series of aryl, h

Synthesis and estrogen receptor binding of 6,7-dihydro-8-phenyl-9-[4-[2-(dimethylamino)ethoxy]phenyl]-5 H-benzocycloheptene, a nonisomerizable analogue of tamoxifen. X-ray crystallographic studies

Syntheses of the title compound, a novel nonisomerizable antiestrogen containing a seven-membered ring, are described. In one method, 6,7-dihydro-9-(4-methoxyphenyl)-5H-benzocycloheptene was brominated at the 8-position and the bromine displaced by phenyl