A novel method of highly enantioselective synthesis of γ-hydroxy-β-keto phosphonates via allene oxides
- 31 December 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (52) , 8543-8544
- https://doi.org/10.1016/s0040-4039(00)61380-1
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Reaction of (R)-pantolactone esters of alpha-bromoacids with amines a remarkable synthesis of optically active alpha-amino estersTetrahedron Letters, 1993
- Reaction of diethyl phosphorochloridite with enolates: a general method for synthesis of .beta.-keto phosphonates and .alpha.-phosphono esters through carbon-phosphorus bond formationThe Journal of Organic Chemistry, 1991
- New synthesis of β-keto phosphonatesTetrahedron Letters, 1989
- The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspectsChemical Reviews, 1989
- A new synthesis of .beta.-keto phosphonates and .beta.-keto silanesThe Journal of Organic Chemistry, 1986
- Horner-wadsworth-emmons reaction: Use of lithium chloride and an amine for base-sensitive compoundsTetrahedron Letters, 1984
- A New, Total Synthesis of Methylenomycin B Using Organic Sulfur and Phosphorus ReagentsSynthesis, 1984
- Direct synthesis of Z-unsaturated esters. A useful modification of the horner-emmons olefination.Tetrahedron Letters, 1983
- Michaelis-Arbusow- und Perkow-ReaktionenPublished by Walter de Gruyter GmbH ,1964
- Neue Phosphorsäureester mit pupillenverengender WirkungThe Science of Nature, 1952