Results Diazomethane indeed was found to undergo totally regiospecific cycloaddition to both DFA5 and fluoroallene5p6 to form pyrazolines 1 and 2. 19F NMR analysis of the product mixtures indicated only one product to have formed in each case. Adducts 1 and 2 were extremely labile compounds but could be purified by careful distillation at reduced pressure, and they were characterized spectroscopically.