Highly Efficient and Diastereoselective Construction of Trifluoromethyl‐Containing Spiro[pyrrolidin‐3,2′‐oxindole] by a Catalyst‐free Mutually Activated [3+2] Cycloaddition Reaction

A catalyst‐free self‐catalyzed [3+2] cycloaddition reaction of isatin‐derived α‐(trifluoromethyl)imines with vinylpyridines is reported. The reaction offers a straightforward and atom‐economical procedure for the preparation of a series of 5′‐trifluoromethyl‐spiro[pyrrolidin‐3,2′‐oxindoles] in excellent yields and diastereoselectivities. The reaction mechanism has been investigated by control experiments, DFT calculation of pKa values and the kinetic profiles, revealing that this reaction featured the mutual activation between isatin‐derived α‐(trifluoromethyl)imines and vinylpyridine to generate the reactive species. A catalyst‐free, self‐catalyzed and highly diastereoselective synthesis of spiro[pyrrolidin‐3,2′‐oxindole] through mutual activation of isatin‐derived α‐(trifluoromethyl)imines and vinylpyridines has been developed that provides the desired products in good yields.