Abstract
The corresponding stereoisomeric p-nitrobenzoates were obtained by reaction of the geometrical isomers of 1,3-dimethyl-, 1,2,5-trimethyl-, and 1-tert-butyl-3-methyl-4-hydroxypiperidines with p-nitrobenzoyl chloride. The stereoisomers of the corresponding benzoates were also synthesized from the geometrical isomers of 1,3-dimethyl-4-hydroxypiperidines. The primary conformations of the investigated compounds in solution were established by means of their PMR spectra.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1643–1646, December, 1975.
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Sokolova, T.D., Romanova, K.I., Malina, Y.F. et al. Synthesis and three-dimensional structure of the benzoates and p-nitrobenzoates of the geometrical isomers of substituted 4-hydroxypiperidines. Chem Heterocycl Compd 11, 1391–1394 (1975). https://doi.org/10.1007/BF00764533
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DOI: https://doi.org/10.1007/BF00764533