Investigation of the stereodirection of the Ritter reaction. Crystaline and molecular structures of N-(2-phenethyl)-2,5-dimethyl-4-phenylpiperid-4-ol and N-(2-phenethyl)-2,5-dimethyl-4-phenyl-4-acetamidopiperidine

Authors

  • B. O. Мартиросян A. D. Mndzhoyan Institute of Fine Organic Chemistry, Academy of Sciences of the Republic of Armenia, 375014 Yerevan
  • А. А. Карапетян A. D. Mndzhoyan Institute of Fine Organic Chemistry, Academy of Sciences of the Republic of Armenia, 375014 Yerevan
  • P. C. Вартанян A. D. Mndzhoyan Institute of Fine Organic Chemistry, Academy of Sciences of the Republic of Armenia, 375014 Yerevan
  • Ю. T. Стручков A. D. Mndzhoyan Institute of Fine Organic Chemistry, Academy of Sciences of the Republic of Armenia, 375014 Yerevan

Abstract

The stereodirection of the Ritter reaction of N-(2-phenethyl)-2,5-dimethyl-4-phenylpiperid-4-ol to the corresponding amide has been studied. X-ray analysis has shown that the reaction occurs with retention of the configuration about atom C4 of the piperidine ring.

How to Cite
Martirosyan, V. O.; Karapetyan, A. A.; Vartanyan, R. S.; Struchkov, Yu. T. Chem. Heterocycl. Compd. 1994, 30, 1200. [Khim. Geterotsikl. Soedin. 1994, 1384.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01184885

Published

1994-10-25

Issue

Section

Original Papers