123355-79-3

Upstream product

• 2328-12-3 6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline monohydrochloride 
• 123279-28-7 (1S,4R)-1-(6,7-Dimethoxy-1,2,3,4-tetrahydro-2-isoquinolylcarbonyl)-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>-heptan-3-one 
• 39637-74-6 (1S)-(-)-camphanic chloride 
• 58518-76-6 ((1-(4-chlorophenyl)vinyl)oxy)trimethylsilane 

Downstream Products

• 175416-14-5 (1S,4R)-1-<(1R)-1,2,3,4-tetrahydro-1-<(2S)-2-hydroxy-2-(4-chloro-phenyl)-ethyl>-6,7-dimethoxy-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one 
• 175222-78-3 (1S,4R)-1-<(1R)-1,2,3,4-tetrahydro-1-<(2R)-2-hydroxy-2-(4-chloro-phenyl)-ethyl>-6,7-dimethoxy-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one 
• 175416-25-8 (1S)-1-(4-chlorophenyl)-2-<(1R)-1,2,3,4-tetrahydro-6,7-dimethoxy-1-isoquinolyl>ethanol 
• 175416-22-5 (1R)-1-(4-chlorophenyl)-2-<(1R)-1,2,3,4-tetrahydro-6,7-dimethoxy-1-isoquinolyl>ethanol 
• 1239950-19-6 (1S)-1,2,3,4-Tetrahydro-6,7-dimethoxy-1-(2-phenyl-1-ethyl)-isoquinoline 
• 123279-35-6 (1R)-1,2,3,4-Tetrahydro-6,7-dimethoxy-1-(2-phenyl-1-ethyl)-isoquinoline 
• 129958-89-0 (1S,4R)-1-<(1R)-1-(2-Cyclohexyl-1-ethyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-isoquinolylcarbonyl>-4,7,7-trimethyl-2-oxa-bicyclo<2.2.1>heptan-3-one 
• 129958-90-3 (1S,3R)-1-<(1R)-1,2,3,4-Tetrahydro-6,7-dimethoxy-1-(2-phenyl-1-ethyl)-2-isoquinolyl-methyl>-3-hydroxymethyl-2,2,3-trimethyl-1-cyclopentanol 
• 123279-36-7 (1R)-1-<2-(4-Chlorophenyl)-1-ethyl>-1,2,3,4-tetrahydro-6,7-dimethoxy-isoquinoline 

Relevant academic research and scientific papers

Asymetric Electrophilic α-Amidoalkylation, VII: Generation, Crystal Structure, and Trapping Reactions of a Chiral 6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline Derived N-Acyliminium Ion

The camphanic acid amide 4 has efficiently been oxidized with triphenylcarbenium tetrafluoroborate (3) to yield the chiral N-acyliminium ion 1.Trapping reactions of 1 with the silyl nucleophiles 7a-c and 10a-f proceeded with stereoselective bond formation