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This article is cited in 16 scientific papers (total in 16 papers)
Oxiranes in the Ritter reaction: synthesis of 6,7-(or 5,8-)dimethoxy-3,4-dihydroisoquinolines by a tandem alkylation–cyclization procedure
V. A. Glushkov, Yu. V. Shklyaev
Institute of Technical Chemistry, Ural Branch of the Russian Academy of Sciences, Perm, Russian Federation
Abstract:
Treatment of 1,2- (or 1,4)-dimethoxybenzene with isobutylene oxide and an appropriate nitrile RCN in concentrated sulfuric acid leads to 1-R-6,7-(or 5,8-)dimethoxy-3,3-dimethyl-3,4-dihydroisoquinolines.
Citation:
V. A. Glushkov, Yu. V. Shklyaev, “Oxiranes in the Ritter reaction: synthesis of 6,7-(or 5,8-)dimethoxy-3,4-dihydroisoquinolines by a tandem alkylation–cyclization procedure”, Mendeleev Commun., 8:1 (1998), 17–18
Linking options:
https://www.mathnet.ru/eng/mendc4633 https://www.mathnet.ru/eng/mendc/v8/i1/p17
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