New research progress on 3340-78-1 in 2021. Quality Control of 2-Phenyl-1,2,3,4-tetrahydroisoquinoline, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 3340-78-1, molcular formula is C15H15N, introducing its new discovery.
Iodo-Bodipys were used as organic catalysts for three different photoredox catalytic organic reactions, i.e. the aza-Henry reaction of tetrahydroisoquinoline, oxidation/[3 + 2] cycloaddition/oxidative aromatization tandem reaction between tetrahydroisoquinolines and maleimides, and C-H arylation of heteroarenes with diazonium salts. The organic photocatalysts act as either electron acceptors (reductive quenching) or electron donors (oxidative quenching) in the single electron transfer (SET) of the catalytic cycles. Different from the widely used Ru(bpy)3[PF6]2, Ir(ppy)3, or halo-xanthane photocatalysts (Eosin Y or Rose Bengal), the new organic photocatalysts show strong absorption of visible light and long-lived triplet excited states, which are beneficial for SET, a crucial step for photoredox catalytic organic reactions. Moreover, the molecular structures of the new photocatalysts can be easily modified, as a result the absorption wavelength of the photocatalysts was readily tuned from 529 nm to 630 nm. The three different types of organic reactions are accelerated with the new organic photocatalysts (typical reaction times 1-2 h) compared to that catalyzed by Ru(bpy)3[PF6]2 or Ir(ppy)3 (reaction time: 12-72 h). The C-H arylation of thiophene with phenyl diazonium salts was used to prepare new Bodipy derivatives that show large Stokes shift. Our results are useful for designing of new organic catalysts for photoredox catalytic organic reactions to prepare highly functionalize organic compounds.
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.Quality Control of 2-Phenyl-1,2,3,4-tetrahydroisoquinoline
Reference：
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem