Related Products of 1196-19-6, New research progress on 1196-19-6 in 2021. The appropriate choice of redox mediator can avoid electrode passivation and overpotential, which strongly inhibit the efficient activation of substrates in electrolysis. In a article, 1196-19-6, molcular formula is C9H7BrS, introducing its new discovery.
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：
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem