REACTION OF 3-AROYLAZIRIDINES WITH DIPHENYLCYCLOPROPENONE AND SUBSEQUENT STEREOSPECIFIC 1,3-DIPOLAR CYCLOADDITION OF THE ADDUCTS WITH DIMETHYL 1-CYCLOBUTENE 1,2-DICARBOXYLATE
K. Matsumoto et al., REACTION OF 3-AROYLAZIRIDINES WITH DIPHENYLCYCLOPROPENONE AND SUBSEQUENT STEREOSPECIFIC 1,3-DIPOLAR CYCLOADDITION OF THE ADDUCTS WITH DIMETHYL 1-CYCLOBUTENE 1,2-DICARBOXYLATE, Tetrahedron letters, 36(30), 1995, pp. 5295-5298
Reaction of 3-aroylaziridines with diphenylcyclopropenone provides anh
ydro-3-hydroxy-2,4-diphenyl-6-arylpyrlium hydroxides that undergo ster
eospecific 1,3-dipolar cycloaddition with dimethyl l-cyclobutene 1,2-d
icarboxylate to give the corresponding exo- and endo-adducts depending
on the substituents of the 6-phenyl group.