BEHAVIOR OF PROPARGYL- AND ALLYLPROPARGYL-AMMONIUM SALTS IN AQUEOUS ALKALINE MEDIUM. SYNTHESIS OF 2-METHYL-2-PHENYLBENZISOINDOLINIUM AND 2-METHYL-2-PHENYLISOINDOLINIUM SALTS

DOI: 10.1007/BF01171292

Source and publish data:

Chemistry of Heterocyclic Compounds p. 58 - 62 (1995)

Update date:2022-08-28

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Authors:

Chukhadzhyan, E. O.

Manasyan, L. A.

Chukhadzhyan, El. O.

Shakhatuni, K. G.

Babayan, A. T.

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Article abstract of DOI:10.1007/BF01171292

Methylphenylpropargyl-(3-phenylpropargyl)-ammonium bromide salts are cyclized almost quantitatively under base-catalysis conditions with the formation of 2-methyl-2-phenylbenzisoindolinium bromide.The allyl analog is subject to rearrangement-decomposit

Full text of DOI:10.1007/BF01171292

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