261509-98-2Relevant academic research and scientific papers
Synthesis and phosphorylation of 2,2',7,7'-tetra(phenylamino)-1,1'-binaphthalene
Nifant'ev, Edward E.,Maslennikova, Vera I.,Shelenkova, Lyudmila V.,Levina, Irina I.,Polekhin, Dmitrii M.
, p. 101 - 102 (2009)
The reaction of 2,2',7,7'-tetrahydroxydinaphthylmethane with aniline in the presence of aniline salts involves the rupture of C-C bonds and the elimination of a methylene bridge and is completed by the formation of 2,2',7,7'-tetra(phenylamino)-1,1'-binaph
B(C6F5)3-catalyzed metal-free hydrogenation of naphthylamines
Li, Gen,Liu, Yongbing,Du, Haifeng
supporting information, p. 2875 - 2878 (2015/04/27)
A catalytic metal-free hydrogenation of naphthylamines using B(C6F5)3 as a catalyst was successfully achieved under mild conditions for the first time to furnish a variety of tetrahydronaphthylamines in 88-99% yields.
Amination of oligofunctionalized dinaphthylmethanes: Factors affecting the reaction pathway
Maslennikova, Vera I.,Shelenkova, Lyudmila V.,Serkova, Olga S.,Vasyanina, Larisa K.,Nifantiev, Edward E.
, p. 136 - 149 (2013/01/16)
The reactions of oligofunctionalized 1,1-dinaphthylmethanes with primary amines and ammonia are described. In the reaction of amines with 2,2′,7,7′-tetrahydroxy- and 2,2′-dihydroxy-1,1- dinaphthylmethanes, the replacement of hydroxy groups by amino groups is accompanied by cleavage of C-C bonds and elimination of a methylene unit. The regiodirection of the process is determined by the number and the nature of substituents in the dinaphthylmethane core. The catalytic amination of 2,2′,7,7′-tetrakis(trifluoromethanesulfonyloxy)-1, 1-dinaphthylmethane is not accompanied by destruction of the dinaphthylmethane core. The reaction selectivity and the product structure depend on the nature of the aminating reagent. ARKAT-USA, Inc.
Polyvariant modification of di- and tetrahydroxydinaphthylmethanes
Maslennikova, Vera I.,Serkova, Olga S.,Shelenkova, Lyudmila V.,Vasyanina, Larisa K.,Tarasenko, Dmitrii V.,Nifantiev, Edward E.
experimental part, p. 886 - 889 (2012/03/26)
Modification of di- and tetrahydroxydinaphthylmethanes yielded a new family of aromatic systems differing by the nature, the number, and positions of functional groups and by the mode of fusion of the naphthalene nuclei. The effect of the starting dinaphthylmethane structure on the modification route was demonstrated.
