Chemistry of Heterocyclic Compounds p. 192 - 195 (1994)
Update date:2022-08-16
Topics:
Chukhadzhyan, E. O.
Chukhadzhyan, El. O.
Shakhatuni, K. G.
Manasyan, L. A.
Babayan, A. T.
It has been shown that, under basic catalytic conditions, dimethylpropargylallyl-(1-allyl-3-phenylpropargyl)- and -(1-allyl-3-α-naphthylpropargyl)ammonium salts undergo diene synthesis type intramolecular cyclization to form condensed analogs of isoindolenium and dihydroindolenium salts with an allyl substituent at position 1.
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