Reactions of resonance stabilized anions. XXXII. Electron-transfer processes. XIII. Coupling reactons of tertiary carbanions with .alpha.-substituted nitro alkanes
Radical–nucleophilic substitution (S<sub>RN</sub>1) reactions: preparation and reactions of α-nitrosuiphides
作者:W. Russell Bowman、Geoffrey D. Richardson
DOI:10.1039/p19800001407
日期:——
α-Nitrosulphides were prepared by SRN1 reaction of 2-bromo-2-nitropropane with thiolate anions, and by SN2 attack of sodium 2-nitropropan-2-ide on symmetrical disulphides. The α-nitrosulphides undergo radicalnucleophilic substitution (SRN1) by nitronate, sulphinate, and malonate anions, but not by thiolate anions.