Theoretical study on the transition state of oxaphosphetane formation between ethylidenetriphenylphosphorane and acetaldehyde
- 1 August 1991
- journal article
- Published by Wiley in Heteroatom Chemistry
- Vol. 2 (4) , 465-468
- https://doi.org/10.1002/hc.520020407
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Selected topics of the wittig reaction in the synthesis of natural productsPublished by Springer Nature ,2005
- Molecular modeling of oxaphosphetane intermediates of wittig olefination reactionsHeteroatom Chemistry, 1990
- Electron transfer in the reaction of benzaldehyde with a nonstabilized ylideTetrahedron Letters, 1989
- Kinetic (not equilibrium) factors are dominant in Wittig reactions of conjugated ylidesJournal of the American Chemical Society, 1989
- The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspectsChemical Reviews, 1989
- Substituent effects and the Wittig mechanism: the case of stereospecific oxaphosphetane decompositionJournal of the American Chemical Society, 1988
- Mechanism of the Wittig reaction: the role of substituents at phosphorusJournal of the American Chemical Society, 1988
- Wittig versus Corey-Chaykovsky Reaction. Theoretical study of the reactivity of phosphonium methylide and sulfonium methylide with formaldehydeJournal of the American Chemical Society, 1987
- Stereochemistry and mechanism of the Wittig reaction. Diasteromeric reaction intermediates and analysis of the reaction courseJournal of the American Chemical Society, 1986
- Detailed rate studies on the Wittig reaction of nonstabilized phosphorus ylides via phosphorus-31, proton, carbon-13 NMR spectroscopy. Insight into kinetic vs. thermodynamic control of stereochemistryJournal of the American Chemical Society, 1985