A new application about 4721-98-6

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Application In Synthesis of 6,7-Dimethoxy-1-methyl-3,4-dihydroisoquinoline, you can also check out more blogs about4721-98-6

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Application In Synthesis of 6,7-Dimethoxy-1-methyl-3,4-dihydroisoquinoline. Introducing a new discovery about 4721-98-6, Name is 6,7-Dimethoxy-1-methyl-3,4-dihydroisoquinoline

Nucleophilic difluoromethylation of C=N bonds in heterocycles with difluoromethyl silane reagents

An efficient and straightforward nucleophilic difluoromethylation of CN bonds in heterocycles under the activation of alkylating agents has been developed. Cyclic iminium salts derived from dihydroisoquinolines, quinolines, and pyridines were successfully difluoromethylated with sulfur-based fluoroalkyl silanes affording a series of new difluoromethylated nitrogen-containing heterocyclic compounds.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Application In Synthesis of 6,7-Dimethoxy-1-methyl-3,4-dihydroisoquinoline, you can also check out more blogs about4721-98-6

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