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

Authors

  • Э. O. Чухаджян Institute of Organic Chemistry, Armenian Academy of Sciences, Erevan 375094
  • Эл. O. Чухаджян Institute of Organic Chemistry, Armenian Academy of Sciences, Erevan 375094
  • К. Г. Шахатуни Institute of Organic Chemistry, Armenian Academy of Sciences, Erevan 375094
  • Л. А. Манaсян Institute of Organic Chemistry, Armenian Academy of Sciences, Erevan 375094
  • А. Т. Бабаян Institute of Organic Chemistry, Armenian Academy of Sciences, Erevan 375094

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 intratmolecular cyclization to form condensed analogs of isoindolenium and dihydroindolenium salts with an allyl substituent at position 1.

How to Cite
Chukhadzhyan, É. O.; Chukhadzhyan, Él. O.; Shakhatuni, K. G.; Manasyan, L. A.; Babayan, A. T. Chem. Heterocycl. Compd. 1994, 30, 192. [Khim. Geterotsikl. Soedin. 1994, 213.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01165010

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Published

1994-02-25

Issue

No. 2 (1994)

Section

Original Papers