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Quinindines

I. The synthesis of 2,3-dihydro-β-quinindines (β-Quinindanes) by the pfitzinger reaction

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

It is shown that, together with Β-quinindane-9-carboxylic acid, the condensation of isatin with cyclopentanone in alkaline medium (Pfitzinger reaction) also affords α, α′-dicyclopentylidenecyclopentanone and 3-cyclopentylidene-Β-quinindane-9-carboxylic acid, the structure of which was confirmed by its NMR, IR, and UV spectra.

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Authors and Affiliations

  1. Ordzhonikidze All-Union Scientific-Research Institute of Pharmaceutical Chemistry, Moscow

    L. E. Kholodov, G. P. Syrova, V. G. Yashunskii & Yu. N. Sheinker

Authors
  1. L. E. Kholodov
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  2. G. P. Syrova
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  3. V. G. Yashunskii
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  4. Yu. N. Sheinker
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Kholodov, L.E., Syrova, G.P., Yashunskii, V.G. et al. Quinindines. Chem Heterocycl Compd 6, 75–79 (1970). https://doi.org/10.1007/BF00475430

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  • DOI: https://doi.org/10.1007/BF00475430

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