A Highly Diastereoselective and Enantioselective Ti(OTos)2−TADDOLate-Catalyzed 1,3-Dipolar Cycloaddition Reaction of Alkenes with Nitrones

A highly diastereo- and enantioselective metal-catalyzed 1,3-dipolar cycloaddition reaction of 3-(( E )-2‘-alkenoyl)-1,3-oxazolidin-2-ones with nitrones has been developed. A series of TiX 2 −TADDOLate catalysts are investigated for their effects on the rate and diastereo- and enantioselectivities in the 1,3-dipolar cycloaddition reaction of alkenes with nitrones. The TiCl 2 −TADDOLate catalysts are known to catalyze the 1,3-dipolar cycloaddition reaction of alkenes with nitrones, giving primarily the exo -isomer of the isoxazolidines with an optical purity of up to 60% ee. If the chloride atoms of the catalyst are substituted with more bulky ligands, such as the tosylato ligand, the endo -isomer is obtained with a diastereoselectivity of >90%. The synthetic aspects of this new method are presented by a series of reactions in which diastereoselectivities of >90% are generally obtained and, most remarkably, enantioselectivities of >90% are frequently obtained. The diastereo- and enantioselectivities of the reaction of the alkenes with nitrones can be accounted for by a transition state model directly derived from a TiCl 2 −TADDOLate−3-cinnamoyloxazolidinone intermediate which has recently been isolated and characterized.