Application of 1196-19-6, 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.1196-19-6, Name is 3-(Bromomethyl)benzo[b]thiophene, molecular formula is C9H7BrS. In a article£¬once mentioned of 1196-19-6
Catalytic asymmetric synthesis of 1,1-disubstituted tetrahydro-beta- carbolines by phase-transfer catalyzed alkylations
Efficient catalytic asymmetric synthesis of 1,1-disubstituted tetrahydro-beta-carbolines has been achieved via asymmetric alkylation of 1-cyanotetrahydro-beta-carbolines using a binaphthyl-modified N-spiro-type chiral phase-transfer catalyst. This is a valuable example of hitherto difficult highly enantioselective alkylations at alpha-carbon of the cyano group under phase-transfer conditions.
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 1196-19-6
Reference£º
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem