Synthesis of (R)-{eta(6)-[O-methyl-N-(alpha-methylbenzyl)hydroxyamino]-benzene} chromium tricarbonyl via nucleophilic aromatic substitution of (eta(6)-fluorobenzene) chromium tricarbonyl
Mrg. Da Costa et al., Synthesis of (R)-{eta(6)-[O-methyl-N-(alpha-methylbenzyl)hydroxyamino]-benzene} chromium tricarbonyl via nucleophilic aromatic substitution of (eta(6)-fluorobenzene) chromium tricarbonyl, J CHEM S P1, (21), 2001, pp. 2850-2855
Chiral hydroxylamine chromium tricarbonyl complexes may be prepared in sati
sfactory to reasonable yield via nucleophilic aromatic substitution of the
anion derived from N,O-substituted hydroxylamines and (eta (6)-fluorobenzen
e) chromium tricarbonyl. The enantiomerically pure complex (R)-{eta (6)-[O-
methyl-N-(alpha -methylbenzyl)hydroxyamino]benzene} chromium tricarbonyl 6a
was characterised by X-ray crystallography.