Discovery of 6,7-Dimethoxy-1-methyl-3,4-dihydroisoquinoline

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 4721-98-6

Related Products of 4721-98-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.4721-98-6, Name is 6,7-Dimethoxy-1-methyl-3,4-dihydroisoquinoline, molecular formula is C12H15NO2. In a Article£¬once mentioned of 4721-98-6

Synthesis of multi ring-fused 2-pyridones via an acyl-ketene imine cyclocondensation

Polycyclic ring-fused 2-pyridones (5a-e and 9a-e) have been prepared via a microwave-assisted acyl-ketene imine cyclocondensation. Starting from 3,4-dihydroisoquinolines (4a-b) or 3,4-dihydroharman (8), fused 2-pyridones could be prepared in a one-step procedure. By using either Meldrum’s acid derivatives (1a-d) or 1,3-dioxine-4-ones (7a-b) as acyl-ketene sources, mono- or disubstitution of the fused 2-pyridone ring could be accomplished. As an application of the method, a formal synthesis of the indole alkaloid sempervilam was performed.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 4721-98-6

Reference£º
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem