Rhodium-Catalyzed Asymmetric Ring Opening Reactions of
Oxabicyclic Alkenes: Application of Halide Effects in the
Development of a General Process
Mark Lautens
Keith Fagnou
Dingqiao Yang
10.1021/ja034845x.s001
https://acs.figshare.com/articles/journal_contribution/Rhodium_Catalyzed_Asymmetric_Ring_Opening_Reactions_of_Oxabicyclic_Alkenes_Application_of_Halide_Effects_in_the_Development_of_a_General_Process/3357592
We have demonstrated halide effects in the rhodium-catalyzed asymmetric ring opening reaction
of oxabicyclic alkenes. By employing halide and protic additives, the catalyst poisoning effect of aliphatic
amines is reversed allowing the amount nucleophile to react in high yield and ee. Second, by simply changing
the halide ligand on the rhodium catalyst from chloride to iodide, the reactivity and enantioselectivity of
reactions employing an aromatic amine, malonate or carboxylate nucleophile are dramatically improved.
Third, through the application of halide effects and more forcing reaction conditions, less reactive oxabicycle
[2.2.1] substrates react to generate synthetically useful enantioenriched cyclohexenol products. Application
of these new conditions to the more reactive oxabenzonorbornadiene permits the reaction to be run with
very low catalyst loadings (0.01 mol %).
2003-12-03 00:00:00
ring opening reaction
halide effects
application
enantioenriched cyclohexenol products
nucleophile
reactive
catalyst poisoning effect