30002-00-7

Upstream product

• 1929-29-9 3-(4-methoxyphenyl)propanoic acid 
• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 
• 943-89-5 (E)-3-(4-methoxyphenyl)acrylic acid 

Downstream Products

• 30002-01-8 6,7-dimethoxy-1-(4-methoxyphenethyl)-3,4-dihydroisoquinoline 
• 1443828-55-4 (6,7-dimethoxy-1-(4-methoxyphenethyl)-3,4-dihydroisoquinolin-2(1H)-yl)(phenyl)methanone 
• 1443828-56-5 (3-chlorophenyl)(6,7-dimethoxy-1-(4-methoxyphenethyl)-3,4-dihydroisoquinolin-2(1H)-yl)methanone 
• 1443828-57-6 (3-bromophenyl)(6,7-dimethoxy-1-(4-methoxyphenethyl)-3,4-dihydroisoquinolin-2(1H)-yl)methanone 
• 108704-90-1 6,7-dimethoxy-1-(4-methoxyphenethyl)-1,2,3,4-tetrahydroisoquinoline 

Relevant academic research and scientific papers

Biomimetic Total Synthesis of Dysoxylum Alkaloids

A five-step total synthesis of Dysoxylum alkaloids has been achieved using a biomimetic approach from zanthoxylamide protoalkaloids. The synthesis featured a direct amidation and a Bischler-Napieralski reaction to form the dihydroisoquinoline ring, which

Synthesis and structure activity relationship of tetrahydroisoquinoline- based potentiators of GluN2C and GluN2D containing N-Methyl-D-aspartate receptors

We describe here the synthesis and evaluation of a series of tetrahydroisoquinolines that show subunit-selective potentiation of NMDA receptors containing the GluN2C or GluN2D subunits. Bischler-Napieralski conditions were employed in the key step for the