Preparation of α- and γ-(α-furyl)pyridines

Mixtures of isomeric alkyl-substituted (in the pyridine ring) α- and γ-(α-furyl)-pyridines were obtained in up to ∼40% yields by condensation of furfural and ammonia with several aliphatic ketones and aldehydes (at 370-380 °C with a cadmium calcium phosphate catalyst). The dependence of the yields and structures of the corresponding isomers on the structure of the starting carbonyl compound was examined. Data from the PMR and mass spectra were used to prove the structures of the pyridine bases obtained. © 1981 Plenum Publishing Corporation.

Editors
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Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
3
Language
English
Pages
284-289
Status
Published
Department
-
Number
-
Volume
17
Year
1981
Organizations
  • 1 Patrice Lumumba People's Friendship University, Moscow, 117923, Russian Federation
Keywords
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Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/1497/