Solvolysis of Styryliodonium Salt: Products, Rates, and Mechanisms
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/72/2/72_2_163/_pdf
Reference19 articles.
1. Solvolysis of Cyclohexenyliodonium Salt, a New Precursor for the Vinyl Cation: Remarkable Nucleofugality of the Phenyliodonio Group and Evidence for Internal Return from an Intimate Ion-Molecule Pair
2. Inversion of configuration in nucleophilic vinylic substitutions of (E)-.beta.-alkylvinyliodonium tetrafluoroborates with halides
3. Vinylic SN2 Reaction of 1-Decenyliodonium Salt with Halide Ions
4. In-Plane Vinylic SN2 Substitution and Intramolecular β Elimination of β-Alkylvinyl(chloro)-λ3-iodanes
5. Acetolysis of Styryl and 1-Decenyl Iodonium Salts. Occurrence of Two-Step Mechanism via Vinylenephenonium Ion and One-Step Inversion Mechanism
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