Final Thoughts on Chemistry for 1-Phenyl-1,2,3,4-tetrahydroisoquinoline

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Electric Literature of 22990-19-8. In my other articles, you can also check out more blogs about 22990-19-8

Research speed reading in 2021. Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. An article , which mentions Electric Literature of 22990-19-8, molecular formula is C15H15N. The compound – 1-Phenyl-1,2,3,4-tetrahydroisoquinoline played an important role in people’s production and life., Electric Literature of 22990-19-8

1-Aryl-1,2,3,4-tetrahydroisoquinolines (THIQ) are key intermediates and products in the pharmaceutical industry. A new method involving intramolecular nucleophilic addition of alpha-amino carbanions to in-situ-generated arynes in N-Boc-protected (Boc = tert-butoxycarbonyl) amine substrates is presented for the synthesis of these compounds. Surprisingly, a similar reaction in Lewis-acid-complexed tertiary amines failed. These results have been analysed using quantum chemical calculations on the intermediates involved in the reactions.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Electric Literature of 22990-19-8. In my other articles, you can also check out more blogs about 22990-19-8

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