345229-52-9

Upstream product

• 91-21-4 1,2,3,4-tetrahydroisoquinoline 
• 96155-57-6 1-(4-methoxyphenyl)ethanone O-acetyl oxime 
• 1006061-06-8 (3,7b-dihydro-2H-1,1a-diazacyclopropa[a]naphthalen-1-yl)-(4-methoxyphenyl)methanone 
• 768-60-5 4-methoxyphenylacetylen 

Relevant academic research and scientific papers

Regioselectivity Control in the Oxidative Formal [3 + 2] Annulations of Ketoxime Acetates and Tetrohydroisoquinolines

A novel copper-catalyzed oxidative formal [3 + 2] annulations of ketoxime acetates and tetrohydroisoquinolines for the synthesis of fused pyrazoles and imidazoles has been developed. A broad range of important isoquinoline-fused pyrazole and imidazole pro

2-substituted 5,6-dihydropyrazolo[5,1-alpha]isoquinoline and derivative and synthesis method thereof

The invention mainly relates to a method for synthesizing 2-substituted 5,6-dihydropyrazolo[5,1-alpha]isoquinoline and a derivative thereof. According to the technical scheme, the 2-substituted 5,6-dihydropyrazolo[5,1-alpha]isoquinoline and the derivative

Facile regioselective synthesis of pyrazolo[5,1-α]isoquinolines via ring-opening cyclization/oxidation reactions of stable aroyldiaziridines of 3,4-tetrahydroisoquinoline with alkynes

Newly prepared, stable aroyldiaziridines of 3,4-tetrahydroisoquinolines undergo regioselective cycloaddition reactions with a number of both mono and disubstituted alkynes, affording five-membered ring products which, after oxidative aromatization of the