SYNTHESIS AND SPECTRAL CHARACTERISTICS OF 2-ARYL-6-METHYL- AND 2-ARYL-6-BENZYL-4,8a-DIPHENYLPERHYDRO[1,3,2]DIOXABORININO[5,4-<i>c</i>]PYRIDINES
DOI:
https://doi.org/10.1007/7165Keywords:
N-alkyl-2, 4, 8a-triarylperhydro[1, 3, 2]dioxaborinino[5, 4-c]pyridines, arylboronic acids, 3-(α-hydroxybenzyl)-4-phenyl-γ-piperidols, , mass spectraAbstract
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.How to Cite
Anh, L. T.; Polyanskiy, K. B.; Mamyrbekova, J. A.; Soldatenkov, A. T.; Soldatova, S. A.; Kurilkin, V. V.; Terentiev, P. B. Chem. Heterocycl. Compd. 2008, 44, 1009. [Khim. Geterotsikl. Soedin. 2008, 1253.]
For this article in the English edition see DOI 10.1007/s10593-008-0144-z