Reference of 4721-98-6, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.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
Studies on the Synthesis of Heterocyclic Compounds. Part 875. The Total Stereoselective Retro Mass Spectral Synthesis of (+/-)-Emetine
Addition of 3,4-dihydro-6,7-dimethoxy-1-methylisoquinoline (5) to 3-methoxycarbonyl-1,6,7,11b-tetrahydro-9,10-dimethoxybenzoquinolizin-4-one (4) produced 2-<(3,4-dihydro-6,7-dimethoxy-1-isoquinolyl)methyl>-3-methoxycarbonyl-1,2,3,6,7,11b-hexahydro-9,10-dimethoxybenzoquinolizin-4-one (6A).The same reaction of 3,4-dihydro-1-methyl-9H-pyrido<3,4-b>indole (15) with (4) afforded 2-(3,4-dihydro-9H-pyrido<3,4-b>-1-indolyl)methyl>-1,2,3,6,7,11b-hexahydro-9,10-dimethoxy-3-methoxycarbonylbenzoquinolizin-4-one (16).The former Michael adduct (6A) was converted into (+/-)-emetine (1) in six steps.
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