Influence des substituants sur la tautomerie cycle-chaine en serie hydroxy-5 isoxazoline-2
- 1 January 1976
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 32 (12) , 1369-1373
- https://doi.org/10.1016/0040-4020(76)85012-0
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Hydroxy-5 isoxazolines-2. Tautomerie cycle-chaine.Tetrahedron Letters, 1974
- Stereopopulation control. I. Rate enhancement in the lactonizations of o-hydroxyhydrocinnamic acidsJournal of the American Chemical Society, 1972
- Steric acceleration of a ring closure to an oxazepinone by steric hindranceJournal of Heterocyclic Chemistry, 1971
- Reaction of hydroxylamine with 3,3-disubstituted 2,4-pentanediones. Formation of novel isoxazole derivativesThe Journal of Organic Chemistry, 1969
- Reaction of benzoylacetaldehyde and of benzoylacetone with hydroxylamine. Acetylation of the resulting “oximes”Journal of the Chemical Society D: Chemical Communications, 1969
- Structural studies by nuclear magnetic resonance—XVTetrahedron, 1968
- The gem Effect. II. The Influence of 3-Mono- and 3,3-Disubstitution on the Rates of Solvolysis of Mono-p-bromophenyl GlutarateJournal of the American Chemical Society, 1965
- Ring-Chain Tautomerism.Chemical Reviews, 1963
- Electrophilic Substituent ConstantsJournal of the American Chemical Society, 1958
- XL.—The conditions underlying the formation of unsaturated and of cyclic compounds from halogenated open-chain derivatives. Part I. Products derived from α-halogenated glutaric acidsJournal of the Chemical Society, Transactions, 1921