A new application about 2-Methyl-5-nitroaniline

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Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition, 99-55-8, Name is 2-Methyl-5-nitroaniline, SMILES is NC1=CC([N+]([O-])=O)=CC=C1C, in an article , author is Li, Jianjun, once mentioned of 99-55-8, Recommanded Product: 99-55-8.

Lewis Acid-Catalyzed C(sp(3))-C(sp(3)) Bond Forming Cyclization Reactions for the Synthesis of Tetrahydroprotoberberine Derivatives

An efficient Lewis acid-catalyzed C(sp(3))-C(sp(3)) bond forming annulation reaction has been developed. This strategy serves as a new method for the facile synthesis of tetrahydro-5H-isoquinolino[2,1-g][1,6] naphthyridine derivatives. A wide range of 2-methylquinoline-3-carbaldehydes and 1,2,3,4-tetrahydroisoquinolines can be applied for this process to afford structurally diverse tetrahydroprotoberberine derivatives in excellent yields.

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Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem