Extended knowledge of 3340-78-1

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Chemistry is traditionally divided into organic and inorganic chemistry. Recommanded Product: 2-Phenyl-1,2,3,4-tetrahydroisoquinoline, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent£¬Which mentioned a new discovery about 3340-78-1

Reactivity and mechanistic insight into visible-light-induced aerobic cross-dehydrogenative coupling reaction by organophotocatalysts

With visible-light irradiation, a mild, simple, and efficient metal-free photocatalytic system for the facile construction of sp3-sp 3 C-C bonds between tertiary amines and activated C-H bonds has been achieved. Spectroscopic study and product analysis demonstrate for the first time that photoinduced electron transfer from N-aryl tetrahydroisoquinolines to eosin Y bis(tetrabutylammonium salt) (TBA-eosin Y) takes place to generate TBA-eosin Y radical anion, which can subsequently react with nucleophiles and molecular oxygen. More strikingly, electron spin resonance (ESR) measurements provide direct evidence for the formation of superoxide radical anions (O 2) rather than singlet oxygen (1O 2) during visible-light irradiation. This active species is therefore believed to be responsible for the large rate of acceleration of the aerobic photocatalytic reactions. Light work: With visible-light irradiation (lambda>450 nm), a mild, simple and efficient metal-free photocatalytic system for the facile construction of sp3-sp3 C-C bonds between tertiary amines and activated C-H bonds has been achieved (see scheme). Electron spin resonance measurements offer direct evidence for the formation of superoxide radical anions (O2) during visible-light irradiation. Copyright

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