97611-71-7

Upstream product

• 91-16-7 1,2-dimethoxybenzene 
• 64-17-5 ethanol 
• 611-71-2 MANDELIC ACID 
• 97611-70-6 ethyl α-methylthio-α-phenyl-3,4-dimethoxyphenylacetate 
• 50766-67-1 2-(3,4-dimethoxyphenyl)-1,3-dithiane 
• 1569272-05-4 (2-(3,4-dimethoxyphenyl)-1,3-dithian-2-yl)(phenyl)methanol 
• 62762-70-3 1-(3,4-dimethoxyphenyl)-2-hydroxy-2-phenylethanone 
• 122-51-0 orthoformic acid triethyl ester 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 75280-06-7 ethyl α-(methylthio)phenylacetate 

Downstream Products

• 633301-45-8 diethyl 2-(3,4-dimethoxyphenyl)-2-phenylhexanedioate 
• 135714-83-9 diethyl 2-(3,4-dimethoxyphenyl)-2-phenylpentane-1,5-dioate 
• 135714-91-9 N-benzyl-2,3,4,5-tetrahydro-7,8-dimethoxy-1-phenyl-1,4-methano-1H-3-benzazepine 
• 135715-08-1 (+/-)-10-amino-6,7,8,9-tetrahydro-2,3-dimethoxy-9-phenyl-6,9-methano-5H-benzocycloheptene hydrochloride 
• 135715-02-5 2,3,4,5-tetrahydro-7,8-dihydroxy-1-phenyl-1,4-ethano-1H-3-benzazepine hydrobromide 
• 135715-10-5 (+/-)-10-amino-6,7,8,9-tetrahydro-9-phenyl-6,9-methano-5H-benzocycloheptene-2,3-diol hydrobromide 
• 135714-93-1 2,3,4,5-tetrahydro-7,8-dihydroxy-1-phenyl-1,4-methano-1H-3-benzazepine hydrobromide 
• 135715-14-9 (9S,10R)-(+/-)-6,7,8,9-tetrahydro-2,3-dimethoxy-9-phenyl-6,9-methano-5H-benzocyclohepten-10-yl toluene-p-sulphonate 
• 135714-88-4 N-benzyl 3-bromo-1,2,3,4-tetrahydro-6,7-dimethoxy-4-oxo-1-phenylnaphthalene-1-carboxamide 
• 135714-89-5 N-benzyl-2,3,4,5-tetrahydro-7,8-dimethoxy-1-phenyl-1,4-methano-1H-3-benzazepine-2,5-dione 
• 135715-07-0 (+/-)-6,7,8,9-tetrahydro-2,3-dimethoxy-9-phenyl-10-trifluoroacetylamino-6,9-methano-5H-benzocyclohepten-5-one 
• 135714-97-5 N-benzyl-6,7,8,9-tetrahydro-2,3-dimethoxy-5-oxo-9-phenyl-5H-benzocycloheptene-6-carboxamide 
• 135714-87-3 N-benzyl 1,2,3,4-tetrahydro-6,7-dimethoxy-4-oxo-1-phenylnaphthalene-1-carboxamide 
• 135714-90-8 N-benzyl-2,3,4,5-tetrahydro-7,8-dimethoxy-1-phenyl-1,4-methano-1H-3-benzazepin-2-one 

Relevant academic research and scientific papers

Synthesis of chiral α-diarylacetic esters by stereospecific 1,2-aryl migration promoted by in situ generated acetals from benzoins

A simple protocol for the synthesis of α-diarylacetic esters from benzoins is described. In situ generated acetal assists rapid 1,2-aryl migration in a stereospecific manner, paving the way to make enantioenriched α-diarylacetic esters from easily accessi

Bridged-ring Nitrogen Compounds. Part 10. Synthesis of Bridged 3-Benzazepine Derivatives as Conformationally Restricted Dopamine Analogues

Ethyl 3,4-dimethoxyphenyl(phenyl)acetate 7, (R=Et), made by an improved procedure, was converted into ethyl 1,2,3,4-tetrahydro-6,7-dimethoxy-4-oxo-1-phenylnaphthalene-1-carboxylate 15 which was used both in a synthesis of 2,3,4,5-tetrahydro-7,8-dihydroxy-