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

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. © 2008 Springer Science+Business Media, Inc.

Authors
Anh L.T. 1 , Polyanskiy K.B.2 , Mamyrbekova J.A.3 , Soldatenkov A.T. 1 , Soldatova S.A. 1 , Kurilkin V.V. 1 , Terentiev P.B.4
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
8
Language
English
Pages
1009-1015
Status
Published
Volume
44
Year
2008
Organizations
  • 1 Peoples' Friendship University of Russia, Moscow 117198, Russian Federation
  • 2 ChemBridge Corporation, Moscow 119048, Russian Federation
  • 3 Abobo-Adjame University, Abidjan, Cote d'Ivoire
  • 4 M. V. Lomonosov Moscow State University, Moscow 119899, Russian Federation
Keywords
3-(α-hydroxybenzyl)-4-phenyl-γ-piperidols; Arylboronic acids; Mass spectra; N-alkyl-2,4,8a-triarylperhydro[1,3,2]dioxaborinino[5,4-c]pyridines
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/3079/
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