Abstract
A Stork reaction — intramolecular transamination — alkylation tandem protocol was used to synthesize functionalized partially hydrogenated quinolines. The molecular and crystal structures of 5-(4-methoxyphenyl)-8,8-dimethyl-6-oxo-2,5,6,7,8,9-hexahydro-1H-thiazolo[3,2-a]quinoline-4-carbonitrile, 9-allyl-3-amino-7,7-dimethyl-5-oxo-4-phenyl-4,5,6,7,8,9-hexahydrothieno[2,3-b]quinoline-2-carbonitrile, and 3-amino-4-(2,5-dimethoxyphenyl)-N-phenyl-5,6,7,8-tetrahydrothieno[2,3-b]quinoline-2-carboxamide were studied by X-ray diffraction analysis.
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Russian Text © The Author(s), 2019, published in Zhurnal Organicheskoi Khimii, 2019, Vol. 55, No. 8, pp. 1273–1286.
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Dyachenko, I.V., Kalashnik, I.N., Dyachenko, V.D. et al. Synthesis of Functionalized Partially Hydrogenated Quinolines by a Stork Reaction — Intramolecular Transamination — Alkylation Tandem Protocol. Russ J Org Chem 55, 1177–1188 (2019). https://doi.org/10.1134/S1070428019080177
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DOI: https://doi.org/10.1134/S1070428019080177