Concepedia

Electroorganic Chemistry. XXVI. Electrooxidation of Enamines, Haloolefins, and Enol Ethers

Tatsuya Shono, Yoshihiro Matsumura, Hiroshi Hamaguchi, Tamotsu Imanishi, Kaoru Yoshida

Bulletin of the Chemical Society of Japan · 1978 · 44 citations · 5 references

DOI

Concepts

Abstract

Abstract Electrooxidation of enamines in methanol afforded two types of methoxylated enamines. Similar treatment of enol ethers gave trimethoxylated compounds. The products formed by the electrolysis of haloolefins in acetic acid were α-acetoxy haloolefins and α-acetoxy ketones.

References

5

Electroorganic chemistry. XXI. Selective formation of .alpha.-acetoxy ketones and general synthesis of 2,3-disubstituted 2-cyclopentenones through the anodic oxidation of enol acetates

Tatsuya Shono, Masahisa Okawa, Ikuzo Nishiguchi · Journal of the American Chemical Society · 1975 · 71 citations

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Electroorganic chemistry. X. Anodic allylic substitution

Tatsuya Shono, Akihiko Ikeda · Journal of the American Chemical Society · 1972 · 67 citations

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Electroorganic chemistry. XII. Anodic oxidation of enol esters

Tatsuya Shono, Yoshihiro Matsumura, Yukio Nakagawa · Journal of the American Chemical Society · 1974 · 54 citations

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Electroorganic chemistry. XIX. Anodic oxidation of nonconjugated dienes

Tatsuya Shono, Akihiko Ikeda, Jun‐ichiro Hayashi et al. · Journal of the American Chemical Society · 1975 · 39 citations

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The Chemistry of the Acetylenes. I. The Preparation of 1-Heptyne by Dehalogenation Methods

G. Bryant Bachman, Arthur J. Hill · Journal of the American Chemical Society · 1934 · 15 citations

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