Research speed reading in 2021. An article , which mentions Safety of 2-Phenyl-1,2,3,4-tetrahydroisoquinoline, molecular formula is C15H15N. The compound – 2-Phenyl-1,2,3,4-tetrahydroisoquinoline played an important role in people’s production and life., Safety of 2-Phenyl-1,2,3,4-tetrahydroisoquinoline
Reported is the controllable selectivity syntheses of four distinct products from the same starting materials by visible-light photoredox catalysis. By employing a dicyanopyrazine-derived chromophore (DPZ) as photoredox catalyst, an aerobic radical mechanism has been developed, and allows the reactions of N-tetrahydroisoquinolines (THIQs) with N-itaconimides to through four different pathways, including addition-cyclization, addition-elimination, addition-coupling, and addition-protonation, with satisfactory chemoselectivity. The current strategy provide straightforward access to four different but valuable N-heterocyclic adducts in moderate to excellent yields. Radical control: A radical mechanism for N-tetrahydroisoquinolines (THIQ) in the presence of oxygen was successfully accomplished by employing a dicyanopyrazine-derived chromophore (DPZ) as a photoredox catalyst. The substrates can undergo either addition-cyclization, addition-elimination, addition-coupling, or addition-protonation by judiciously regulating the reaction conditions. Four types of N-heterocycles are generated in moderate to excellent yields.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 3340-78-1, and how the biochemistry of the body works.Safety of 2-Phenyl-1,2,3,4-tetrahydroisoquinoline
Reference：
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem