Preparation of Enolates from α-Haloketones with n-BuLi, PhMgBr, or Et2Zn via Halogen-Metal Exchange Reaction
- 1 June 1995
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 24 (6) , 463-464
- https://doi.org/10.1246/cl.1995.463
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- One-pot synthesis of α,β-unsaturated ketones from tert-butyldimethylsilyldibromomethane and two different aldehydesTetrahedron Letters, 1994
- Trialkylborane as an Initiator and Terminator of Free Radical Reactions. Facile Routes to Boron Enolates via α-Carbonyl Radicals and Aldol Reaction of Boron EnolatesBulletin of the Chemical Society of Japan, 1991
- Samarium-catalyzed intramolecular Tishchenko reduction of .beta.-hydroxy ketones. A stereoselective approach to the synthesis of differentiated anti 1,3-diol monoestersJournal of the American Chemical Society, 1990
- Preparation and reactions of an alkylzinc enolateOrganometallics, 1987
- Stereoselective aldol condensations via boron enolatesJournal of the American Chemical Society, 1981
- Acyclic stereoselection. 7. Stereoselective synthesis of 2-alkyl-3-hydroxy carbonyl compounds by aldol condensationThe Journal of Organic Chemistry, 1980