Ring-Chain Tautomerism in Anions Derived from Substituted (Arylideneamino)toluenes and (Arylideneamino)oxindoles

DOI: 10.1021/jo00163a006

Source and publish data:

Journal of Organic Chemistry p. 2468 - 2472 (1983)

Update date:2022-08-04

Topics: Anions NMR spectroscopy Isolation Derivatives Proton transfer Substituted UV-Vis Spectroscopy Oxindoles Ring-chain tautomerism Arylideneamino

Authors:

Goetz, Frederick J.

Hirsch, Jerry A.

Augustine, Robert L.

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Article abstract of DOI:10.1021/jo00163a006

Intramolecular nucleophilic attack by carbon and nitrogen anions on imine and enone double bonds, respectively, has been investigated as a synthetic route to fused five-membered azacycles.In both (arylideneamino)toluenes and (arylideneamino)oxindoles, cyc

Full text of DOI:10.1021/jo00163a006

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