Electroorganic chemistry. 62. Reaction of iminium ion with nucleophile: a versatile synthesis of tetrahydroquinolines and julolidines
…, Y Matsumura, K Inoue, H Ohmizu…
Index: Shono, Tatsuya; Matsumura, Yoshihiro; Inoue, Kenji; Ohmizu, Hiroshi; Kashimura, Shigenori Journal of the American Chemical Society, 1982 , vol. 104, # 21 p. 5753 - 5757
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Citation Number: 89
Abstract
Abstract: A versatile synthetic method of tetrahydroquinolines and julolidines has been developed. The method involves the anodic oxidation of N, N-dimethylaniline in methanol to afford a-methoxylated or a, &-dimethoxylated compounds and subsequent treatment of the products with Lewis acids in the presence of nucleophiles. Simple and electron-rich olefins such as alkenes, styrene, enol ethers, silyl enol ethers, enamines, and enol esters are ...
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