DIRECT OBSERVATION OF ORTHOGONAL ORIENTATION OF AN AROMATIC RING ATTACHED TO THE CARBENE CARBON IN FISCHER CARBENE COMPLEXES IN SOLUTION - DIASTEREOTOPICITY OF BENZYL PROTONS AS A STEREOCHEMICAL PROBE
Sr. Amin et al., DIRECT OBSERVATION OF ORTHOGONAL ORIENTATION OF AN AROMATIC RING ATTACHED TO THE CARBENE CARBON IN FISCHER CARBENE COMPLEXES IN SOLUTION - DIASTEREOTOPICITY OF BENZYL PROTONS AS A STEREOCHEMICAL PROBE, Organometallics, 15(16), 1996, pp. 3528-3533
Diastereotopicity of methylene protons of benzyloxy and benzylamino gr
oups in Fischer carbene complexes serves as a stereochemical probe to
reveal orthogonal orientation of the aromatic rings attached to the ca
rbene carbon with respect to the metal-carbene pi-plane in solution.