EFFECT OF THE ALPHA-ALKYL SUBSTITUENT OF CONJUGATED NITROOLEFINS ON THE FORMATION OF CYCLIC NITRONIC ESTERS VS NITROCYCLOPROPANES IN THEIR REACTION WITH SULFUR YLIDES
G. Kumaran et Gh. Kulkarni, EFFECT OF THE ALPHA-ALKYL SUBSTITUENT OF CONJUGATED NITROOLEFINS ON THE FORMATION OF CYCLIC NITRONIC ESTERS VS NITROCYCLOPROPANES IN THEIR REACTION WITH SULFUR YLIDES, Synthesis, (12), 1995, pp. 1545
The formation of cyclic nitronic esters (isoxazoline N-oxides) vs. nit
rocyclopropanes in the reaction of conjugated nitroolefins with sulfur
ylides depends on the presence of an alpha-alkyl substituent in the c
onjugated nitroolefins.