Chiral dirhodium(II) compounds, Rh 2 (O 2 CR) 2 (pc) 2 (pc = ortho-metalated arylphosphine), with a head-to-tail arrangement ( 1 − 21 ) are used in the cyclopropanation of α-diazo ketones. The influence of catalyst ligands and substrate structure on enantioselectivity is studied. Temperature and solvent dependence assays are performed, the best ee values being obtained in refluxing pentane. Results compare favorably with those reported in the literature using Ru, Cu, and other Rh(II) catalysts.
No takes yet. Share an insight, caveat, or question.
Barberis et al. (2002) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: