Top Picks: new discover of 17680-55-6

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.COA of Formula: C9H10BrN, you can also check out more blogs about17680-55-6

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. COA of Formula: C9H10BrN. Introducing a new discovery about 17680-55-6, Name is 7-Bromo-1,2,3,4-tetrahydroisoquinoline

Oxidation-Induced beta-Selective C-H Bond Functionalization: Thiolation and Selenation of N-Heterocycles

Site-selective intermolecular C-H bond functionalization is of central importance to synthetic chemistry. In particular, direct beta-functionalization of N-heterocycles still remains a great challenge. Herein, we develop a strategy for oxidation-induced thiolation and selenation at the beta-position of piperidine derivatives and 1,2,3,4-tetrahydroisoquinoline via C-H bond functionalization. Various 4-sulfenylisoquinolines, 3-sulfenylpyridines, and 4-selenylisoquinolines can be obtained by using O2 as the only oxidant. Notably, neither a directing group nor a metal catalyst is necessary in this transformation. The preliminary mechanistic studies revealed that the oxidation and rearrangement pathway were key steps in this transformation, which provides a meaningful strategy for controlling site selectivity in the beta-functionalization of N-heterocycles.

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.COA of Formula: C9H10BrN, you can also check out more blogs about17680-55-6

Reference£º
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem