Tris(phenylthio)methyllithium as a formyl anion equivalent in conjugate addition. Preparation of unprotected γ-ketoaldehydes.
- 31 December 1978
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 19 (38) , 3533-3536
- https://doi.org/10.1016/s0040-4039(01)94985-8
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- N-Nitromethylphthalimide. A formyl anion equivalentCanadian Journal of Chemistry, 1977
- Reactions in dry media. A simple conversion of nitro groups into carbonylsJournal of the American Chemical Society, 1977
- Umpolung of the Reactivity of Carbonyl Compounds Through Sulfur-Containing ReagentsSynthesis, 1977
- New horizons in carbonyl chemistry: reagents for nucleophilic acylationTetrahedron, 1976
- Copper(I)-promoted thiophenoxide ionization in solution. Simple synthesis of vinyl phenyl sulfidesThe Journal of Organic Chemistry, 1975
- Synthesis of Jasmonoids, a ReviewSynthetic Communications, 1974
- Synthesis of (±) 11-deoxyprostaglandin E1, Fα and F 1β and its 15β-epimers by conjugate addition of nitromethane to 2-(6′-carbomethoxyhexyl)-2-cyclopenten-1-oneTetrahedron Letters, 1973
- New method for the conversion of nitro groups into carbonylsThe Journal of Organic Chemistry, 1973
- Methods for the Synthesis of 3-OxocyclopentenesSynthesis, 1973
- Prostaglandins - a new total synthesis of (±)-11-deoxyprostaglandinsTetrahedron Letters, 1972