Zhang, Shilong; Liu, Yungen; Xing, Fangrong; Che, Chi-Ming published the artcile< Direct preparation of unprotected aminimides (R3N+-NH-) from natural aliphatic tertiary alkaloids (R3N) by [Mn(TDCPP)Cl]-catalysed N-amination reaction>, Synthetic Route of 6882-68-4, the main research area is unprotected aminimide preparation antitumor human; natural aliphatic tertiary alkaloid amination manganese complex catalyst; manganese complex preparation.
A panel of natural aliphatic tertiary alkaloids were directly converted to unprotected aminimides via [Mn(TDCPP)Cl]-catalyzed N-amination reaction using O-(2,4-dinitrophenyl)hydroxylamine as the nitrogen source in up to 98% yields under mild reaction conditions.
Chemical Communications (Cambridge, United Kingdom) published new progress about Alkaloids Role: PAC (Pharmacological Activity), PRP (Properties), RCT (Reactant), SPN (Synthetic Preparation), THU (Therapeutic Use), BIOL (Biological Study), RACT (Reactant or Reagent), PREP (Preparation), USES (Uses). 6882-68-4 belongs to class naphthyridine, and the molecular formula is C15H24N2O, Synthetic Route of 6882-68-4.
Referemce:
1,8-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N2 – PubChem