Abstract
Aryl-N-methyl-and aryl-N-benzyl-B-substituted 4,8a-diphenylperhydro[1,3,2]dioxaborinino[5,4-c]pyridines, which are representatives of a new class of bicyclic compounds containing four heteroatoms, were synthesized from N-methyl-and N-benzyl-3-(α-hydroxybenzyl)-4-phenyl-γ-piperidols by cyclocondensation with arylboronic acids. The 1H NMR and mass spectra of these compounds were examined as well as mass spectra of previously obtained analogs.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1253–1259, August, 2008.
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Anh, L.T., Polyanskiy, K.B., Mamyrbekova, J.A. et al. Synthesis and spectral characteristics of 2-aryl-6-methyl-and 2-aryl-6-benzyl-4,8a-diphenylperhydro[1,3,2]dioxaborinino[5,4-c]pyridines. Chem Heterocycl Comp 44, 1009–1015 (2008). https://doi.org/10.1007/s10593-008-0144-z
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DOI: https://doi.org/10.1007/s10593-008-0144-z