Jiang, Wen-Nian; Zhao, Qing-Lan; Cheng, Wen-Shuo; Xiao, Jun-An; Xiang, Hao-Yue; Chen, Kai; Yang, Hua published the artcile< CuI-mediated benzannulation of (ortho-arylethynyl)phenylenaminones to assemble α-aminonaphthalene derivatives>, Recommanded Product: 4-Bromobenzylamine, the main research area is aminonaphthalene preparation; arylethynyl phenylenaminone amine preparation benzannulation copper iodide catalyst.
Simple manipulation of exogenous amines readily offers the structural diversity of the resulting α-aminonaphthalenes II. Preliminary investigation of the photophys. features of the representative as-prepared compounds demonstrated their tunable fluorescence properties. A copper-mediated annulation protocol for new (ortho-arylethynyl)phenyl enaminones I (R = dimethylaminyl, pyrrolidin-1-yl, cyclohexylaminyl, etc.; R1 = H, 4-(C(O)2CH3)C6H4, 4-NCC6H4; R2 = C6H5, 4-(CH2CH3)C6H4, 4-((CH2)2CH3)C6H4, 4-((CH2)3CH3)C6H4, 4-CH3OC6H4, 4-FC6H4) bearing a N,N-dimethylamine moiety was developed to facilely install a series of α-aminonaphthalene derivatives II.
Organic Chemistry Frontiers published new progress about Amines Role: RCT (Reactant), RACT (Reactant or Reagent). 3959-07-7 belongs to class bromides-buliding-blocks, and the molecular formula is C7H8BrN, Recommanded Product: 4-Bromobenzylamine.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary