1H and 13C NMR spectra and three-dimensional structures of 1,2,5-trimethyl-4-phenylaminopiperidine isomers

The three-dimensional structures of two isomers of 1,2,5-trimethyl-4-phenylaminopiperidine were established on the basis of an analysis of their 1H and 13C NMR spectra. The piperidine ring has a chair conformation in both isomers. The δ isomer has the 1,2e,5a, trimethyl-4e-phenylaminopiperidine structure, while the γ isomer has the 1,2e,5e-trimethyl-4e-phenylaminopiperidine structure. © 1983 Plenum Publishing Corporation.

Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
11
Language
English
Pages
1174-1177
Status
Published
Volume
18
Year
1982
Organizations
  • 1 Patrice Lumumba Peoples' Friendship University, Moscow, Russian Federation
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/1443/
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Prostakov N.S., Klochkov A.M., Varlamov A.V.
Chemistry of Heterocyclic Compounds. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Vol. 18. 1982. P. 1177-1181
Mitskiévič N.V., Senin Y.E.
Lettere al Nuovo Cimento. Società Italiana di Fisica. Vol. 35. 1982. P. 419-422