86576-32-1Relevant articles and documents
REGIOCHEMISTRY OF THE DIPOLAR CYCLOADDITIONS OF NITRILE OXIDES TO UNACTIVATED OLEFINS. APPLICATION TO THE STEREOSELECTIVE ELABORATION OF β-HYDROXYCARBONYL COMPOUNDS.
Martin, Stephen F.,Dupre, Brian
, p. 1337 - 1340 (1983)
The 1,3-dipolar cycloadditions of nitrile oxides 1 with Z-disubstituted olefins 2 proceeds with a high degree of regioselectivity to give the isoxazolines 4, whereas addition to E-disubstituted olefins 3 affords mixtures of the isomeric isoxazolines 4 and