This article is cited in 4 papers

Synthesis and phosphorylation of 2,2’,7,7’-tetra(phenylamino)-1,1’-binaphthalene

E. E. Nifantyev^a, V. I. Maslennikova^a, L. V. Shelenkova^a, I. I. Levina^b, D. M. Polekhin<sup>a

a</sup> Department of Chemistry, Moscow State Pedagogical University, Moscow, Russian Federation
^b N.M. Emanuel Institute of Biochemical Physics, Russian Academy of Sciences, Moscow, Russian Federation

Abstract: 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’-binaphthalene, the phosphorylation of which with 2-chloro-1,3,2-dioxaphosphinane and dichloroisopropyl phosphite yields original polycyclic phosphamide architectures.

Language: English

DOI: 10.1016/j.mencom.2009.03.017

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