EFFECT OF THE ALPHA-ALKYL SUBSTITUENT OF CONJUGATED NITROOLEFINS ON THE FORMATION OF CYCLIC NITRONIC ESTERS VS NITROCYCLOPROPANES IN THEIR REACTION WITH SULFUR YLIDES

Authors
KUMARAN G KULKARNI GH
Citation
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
Citations number
34
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synthesis → ACNP
ISSN journal
00397881
Issue
12
Year of publication
1995
Database
ISI
SICI code
0039-7881(1995):12<1545:EOTASO>2.0.ZU;2-K
Abstract
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.