PHOSPHONATION OF 1,1'-BINAPHTHALENE-2,2'-DIOL (BINOL) - SYNTHESIS OF DIHYDROXY-1,1'-BINAPHTHATENE-6,6'-DIYLDIPHOSPHONIC AND DIHYDROXY-1,1'-BINAPHTHATENE-6,6'-DIYLDIPHOSPHONIC ACID
Pa. Jaffres et al., PHOSPHONATION OF 1,1'-BINAPHTHALENE-2,2'-DIOL (BINOL) - SYNTHESIS OF DIHYDROXY-1,1'-BINAPHTHATENE-6,6'-DIYLDIPHOSPHONIC AND DIHYDROXY-1,1'-BINAPHTHATENE-6,6'-DIYLDIPHOSPHONIC ACID, Journal of the Chemical Society. Perkin transactions. I (Print), (13), 1998, pp. 2083-2089
The synthesis of 6,6'-bis(diethoxyphosphoryl)-1,1 '-binaphthalene-2,2'
-diol 1 in racemic and chiral forms is described. This synthesis, whic
h involves a palladium-assisted phosphonation step, allows study of th
e phosphonation of bromophenol as an;electron-rich aryl bromide model.
Furthermore, the synthesis of 2,2'-dihydroxy-1,1 '-binaphthalene-6,6'
-diyldiphosphonic acid 2, from its diester 1, leads to a key intermedi
ate in the synthesis of hybrid organic-inorganic materials.