Conjugate Addition In Phase Transfer Catalysis Conditions: Reactions of α Enones with Arylacetonitriles
- 1 June 1985
- journal article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 15 (8) , 689-696
- https://doi.org/10.1080/00397918508063859
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Michael Addition of Isopropylidene Malonate to Electrophilic Olefins under Phase-Transfer ConditionsSynthesis, 1984
- Addition conjuguee-alkylation: stereochimie de la reaction des lithiens d'arylacetonitriles sur les cyclenones suivie du piegeage par l'iodure de methyle en une seule operationTetrahedron, 1983
- Asymmetric induction in the Michael reaction by means of chiral phase-transfer catalysts derived from cinchona and ephedra alkaloidsJournal of the Chemical Society, Perkin Transactions 1, 1981
- Substituent effects on 1–2 versus 1–4 addition of lithiated arylacetonitriles to 2-cyclohexenones in tetrahydrofuranSynthetic Communications, 1981
- Asymmetric induction in the Michael reactionThe Journal of Organic Chemistry, 1979
- Phase-Transfer Catalysis of the Michael Addition to α,β-Unsaturated AldehydesSynthesis, 1979
- Alkyl effects on equilibrium acidities of carbon acids in protic and dipolar aprotic media and the gas phaseThe Journal of Organic Chemistry, 1978
- Factors controlling the regioselectivity of additions to α-enones—VITetrahedron, 1978
- Phase Transfer Catalysis in Organic SynthesisPublished by Springer Nature ,1977
- Etude de la reactivite des α-enones : V reactions avec le lithien du phenylacetonitrileTetrahedron Letters, 1976