Abstract
Liquid-phase catalytic reduction of 1,2,3-substituted 5,6,7,8-tetrahydroisoquinolinium perchlorates was investigated. The reaction proceeds stereodirectionally affording cis-decahydroisoquinolines. The probable scheme of reaction products formation is suggested. The structure of compounds obtained was established by IR and 13C NMR spectroscopy.
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Original Russian Text © P.V. Reshetov, R.V. Seller, A.G. Golikov, M.I. Skuratova, 2017, published in Zhurnal Organicheskoi Khimii, 2017, Vol. 53, No. 2, pp. 229–232.
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Reshetov, P.V., Seller, R.V., Golikov, A.G. et al. Catalytic synthesis and stereostructure of 1,2,3-trisubstituted decahydroisoquinolines. Russ J Org Chem 53, 222–225 (2017). https://doi.org/10.1134/S1070428017020130
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DOI: https://doi.org/10.1134/S1070428017020130