Abstract
The condensation of 1,2,5-trimethylpiperidine-4-one with phenol and isomeric cresols yields 1,2,5-trimethyl-4-(p-hydroxyphenyl)- and (p-hydroxytolyl)-δ3-tetrahydropyridines, the structure and conformation of which have been studied by proton NMR spectroscopy.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1367–1370, October, 1986.
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Rezakov, V.A., Das, S.K., Fomichev, A.A. et al. 1,2,5-Trimethyl-4-(p-hydroxyaryl)-δ3-tetrahydropyridines and their spatial structure. Chem Heterocycl Compd 22, 1107–1110 (1986). https://doi.org/10.1007/BF00473489
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DOI: https://doi.org/10.1007/BF00473489