Cerium(III) Chloride Promoted Nucleophilic Addition of Organolithium Reagents to α‐Alkyl‐β‐Ketophosphine Oxides: A New Protocol for the Synthesis of Stereochemically Defined Trisubstituted Olefins
- 2 October 1995
- journal article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 34 (18) , 2046-2048
- https://doi.org/10.1002/anie.199520461
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Cerium chloride (III) promoted nucleophilic addition of organolithium reagents to α-diphenylphosphinoyl ketones. An efficient method for the synthesis of horner-wittig intermediatesTetrahedron Letters, 1994
- Phenylthioacetylene as a source of stereodefined trisubstituted alkenesTetrahedron Letters, 1994
- The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspectsChemical Reviews, 1989
- Improved procedure for preparation of optically active 3-hydroxyglutarate monoesters and 3-hydroxy-5-oxoalkanoic acidsThe Journal of Organic Chemistry, 1988
- Horner-Wittig reactions using dibenzophosphole oxides: Stereochemically controlled reduction of ketonesTetrahedron Letters, 1986
- Controlled carbometalation. 20. Carbometalation reaction of alkynes with organoalene-zirconocene derivatives as a route to stereo-and regiodefined trisubstituted alkenesJournal of the American Chemical Society, 1985
- Recent advances in double bond formationPublished by Walter de Gruyter GmbH ,1985
- Synthese de phosphonates β-carbonyles: I. Par voie carbanioniqueJournal of Organometallic Chemistry, 1984
- The wittig-horner route to tri-substituted alkanes : synthesis of -α-bisaboleneTetrahedron Letters, 1983
- Stereoselective and stereospecific olefin synthesisQuarterly Reviews, Chemical Society, 1971