Electroorganic Chemistry. XXVI. Electrooxidation of Enamines, Haloolefins, and Enol Ethers
- 1 July 1978
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 51 (7) , 2179-2180
- https://doi.org/10.1246/bcsj.51.2179
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.This publication has 6 references indexed in Scilit:
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