Oxidative reactions of azines. 1. Ketohydroxylation of 4-phenyl-1,2,5,6-tetrahydropyridines. Synthesis and structure of 3,4-dihydroxy-4-phenylpiperidin-2-ones and their acetoxy derivatives

N-Alkyl substituted 4-phenyl-1,2,5,6-tetrahydropyridines which do not undergo Wagner hydroxylation are converted in good yields to the corresponding 3,4-dihydroxy-2-oxo-pipendines under modified conditions for this reaction. The molecular structures of a 3,4-dihydroxy-4-phenyl-pipendin-2-one and its diacetatate have been studied by x-ray crystalographic analysis. ©1996 Plenum Publishing Corporation.

Editors
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Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
2
Language
English
Pages
197-201
Status
Published
Department
-
Number
-
Volume
32
Year
1996
Organizations
  • 1 Russian University of National Friendship, Moscow 117198, 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/843/