Abstract
8-Carboxamido- and 8-phthalimido-2.2,6,6-tetramethylquinuclidines were synthesized. The effect of α,α′-gem-dimethyl groups, which shield the nitrogen atom, on the synthesis of functionally substituted quinuclidine compounds by classical methods was studied.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 927–934, July, 1976.
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Levkoeva, E.I., Yakhontov, L.N. Synthesis of 2.2,6,6-tetramethylquinucltdines with functional substituents in the quinuclidine ring. Chem Heterocycl Compd 12, 770–775 (1976). https://doi.org/10.1007/BF00477010
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DOI: https://doi.org/10.1007/BF00477010