DYNAMIC EQUILIBRATION OF DIASTEREOMERIC SALTS OF ATROPISOMERS - PROTON NMR-SPECTRA OF 1,8-DI(3'-PYRIDYL)NAPHTHALENE IN THE PRESENCE OF R-CAMPHORSULFONIC ACID
Nm. Maier et Ja. Zoltewicz, DYNAMIC EQUILIBRATION OF DIASTEREOMERIC SALTS OF ATROPISOMERS - PROTON NMR-SPECTRA OF 1,8-DI(3'-PYRIDYL)NAPHTHALENE IN THE PRESENCE OF R-CAMPHORSULFONIC ACID, Tetrahedron, 53(2), 1997, pp. 465-468
In the presence of chiral camphorsulfonic acid (CSA) the anti and syn
atropisomers of the title compound in acetone-d(6) form diastereomeric
salts detectable at ambient temperatures by proton NMR. Comparison of
these spectra with those generated in the presence of racemic CSA pro
vides evidence for the formation of the diastereomers. Copyright (C) 1
996 Elsevier Science Ltd