INVESTIGATIONS ON DIASTEREOISOMERIC TETRAORGANOTIN COMPOUNDS - THE USE OF SN-119 NMR-SPECTROSCOPY FOR THE DIRECT DETERMINATION OF THE DIASTEREOISOMERIC COMPOSITION
J. Klein et al., INVESTIGATIONS ON DIASTEREOISOMERIC TETRAORGANOTIN COMPOUNDS - THE USE OF SN-119 NMR-SPECTROSCOPY FOR THE DIRECT DETERMINATION OF THE DIASTEREOISOMERIC COMPOSITION, Perkin transactions. 2, (12), 1994, pp. 2523-2524
The distinction of enantiomeric alkyl halides by conversion in non-ass
ociating diastereoisomeric tetraorganostannanes of the type R(2)Sn R'(
2) (R = Ph, Bu and R' = 2-octyl, 2-butyl, but-3-en-2-yl, 2-methylbutyl
) using Sn-119 NMR spectroscopy is described. An 119Sn ''inverse gated
decoupling'' technique makes the direct quantitative analysis of the
diastereoisomeric composition feasible. C-13 NMR data are reported and
a diastereotopic non-equivalence of the R groups in the meso-derivati
ves of R(2)SnR'(2) is described. Achiral diorganotin dichlorides were
used as derivatizing agents.