Nucleophilic substitution reaction of α-siloxyamines with organometallics: a new method for α-substitution of tertiary amines via their n-oxides
- 31 December 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (41) , 4677-4680
- https://doi.org/10.1016/s0040-4039(01)91231-6
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- A convenient synthesis of unsymmetrical secondary amines. formation of unstable formaldehyde imines.Tetrahedron Letters, 1984
- Dipole-stabilized carbanions: the .alpha.' lithiation of piperididesJournal of the American Chemical Society, 1984
- Base-promoted rearrangement of siloxyammonium salts: a new method of dealkylation of tertiary amines via their N-oxidesJournal of the Chemical Society, Chemical Communications, 1984
- Alkylation of the isoquinoline skeleton in the 1-positionTetrahedron, 1983
- Asymmetric alkylation of α-amino carbanions. An enantioselective synthesis of (S)-1-alkyl-1,2,3,4-tetrahydroisoquinolinesJournal of the American Chemical Society, 1983
- Electroorganic chemistry. 46. A new carbon-carbon bond forming reaction at the .alpha.-position of amines utilizing anodic oxidation as a key stepJournal of the American Chemical Society, 1981
- Umpolung of Amine Reactivity. Nucleophilic α‐(Secondary Amino)‐alkylation via Metalated NitrosaminesAngewandte Chemie International Edition in English, 1975