Electric Literature of 1612-65-3, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 1612-65-3, Name is 2-Methyl-1,2,3,4-tetrahydroisoquinoline, molecular formula is C10H13N. In a Article£¬once mentioned of 1612-65-3
Oxidation of Trialkylamines by BrCCl3: Scope, Applications and Mechanistic Aspects
The catalyst-free photochemical reaction of trialkylamines and BrCCl3 induced by visible light was investigated. The outcome of the reaction was found to depend strongly on the nature of the amine substrates. N-Methyl-1,2,3,4-tetrahydroisoquinolines give 3,4-dihydroisoquinolinium salts, whereas aliphatic trialkylamines produce hydrohalide salts and streptocyanines as the major products. The addition of KCN inhibits streptocyanine formation, and results in the clean formation of alpha-aminonitriles instead. The light-absorbing species and the underlying reaction mechanism were studied by DFT calculations and experimental observations.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Electric Literature of 1612-65-3. In my other articles, you can also check out more blogs about 1612-65-3
Reference£º
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem