Generation of the enolate of succinic anhydride in the presence of carbonyl compounds. A facile preparative method of β-methoxycarbonyl γ-substituted γ-butyrolactones
- 31 December 1977
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 18 (17) , 1423-1424
- https://doi.org/10.1016/s0040-4039(01)93062-x
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Geminal acylation via pinacol rearrangement. Synthesis of spiro[4.n] ring systemsJournal of the American Chemical Society, 1977
- A convenient method for the preparation of β-hydroxy estersTetrahedron Letters, 1976
- Regiospecific directed aldol reactions of methyl ketones with aldehydesTetrahedron Letters, 1976
- An efficient method for the preparation of 1,1-bis(trimethylsilyl)alkan-1-olTetrahedron Letters, 1976
- Synthetic routes to polyfunctional molecules via metallated N,N-dimethylhydrazonesTetrahedron Letters, 1976
- Quaternary ammonium enolates as synthetic intermediates. Regiospecific alkylation reaction of ketonesJournal of the American Chemical Society, 1975
- Trimethylsilylacetic acid dianion: application to organic synthesisJournal of the Chemical Society, Chemical Communications, 1975
- New cross-aldol reactions. Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachlorideJournal of the American Chemical Society, 1974
- Regiospecific aldol condensations of the kinetic lithium enolates of methyl ketonesThe Journal of Organic Chemistry, 1974
- Chemistry of carbanions. XXIII. Use of metal complexes to control the aldol condensationJournal of the American Chemical Society, 1973