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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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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DOI: https://doi.org/10.1007/BF01165010