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218. Intramolecular cyclization of an ammonium salt containing an allyl substituent in position 1 of the diene fragment

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Chemistry of Heterocyclic Compounds Aims and scope

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Abstract

It has been shown that, under basic catalytic conditions, dimethylpropargylallyl-(1-allyl-3 phenylpropargyl)- and-(1-allyl-3-α-naphthylpropargyl)atnmoniutn salts undergo diene synthesis type intratnolecular cyclization to form condensed analogs of isoindolenium and dihydroitulolenium salts with an allyl substituent at position 1.

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Authors and Affiliations

  1. Institute of Organic Chemistry, Armenian Academy of Sciences, 375094, Yerevan

    É. O. Chukhadzhyan, Él. O. Chukhadzhyan, K. G. Shakhatuni, L. A. Manasyan & A. T. Babayan

Authors
  1. É. O. Chukhadzhyan
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  2. Él. O. Chukhadzhyan
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  3. K. G. Shakhatuni
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  4. L. A. Manasyan
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  5. A. T. Babayan
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 213–216, February, 1994. Original article submitted October 12, 1993.

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Chukhadzhyan, É.O., Chukhadzhyan, É.O., Shakhatuni, K.G. et al. 218. Intramolecular cyclization of an ammonium salt containing an allyl substituent in position 1 of the diene fragment. Chem Heterocycl Compd 30, 192–195 (1994). https://doi.org/10.1007/BF01165010

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