Beckmann Rearrangement of 2-Hydroxy-5-Methylacetophenone Oxime using Vilsmeier-Haack Reagent (POCl3/ DMF): Synthesis of Some New Heterocycles

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Abstract

Synthesis of some new heterocyclic derivatives 3a-3g has been reported by the condensation of suitable reagents with malondialdehyde 2. The malondialdehyde 2 was synthesized by Beckmann rearrangement of 2-hydroxy-5-methylacetophenone oxime 1 using Vilsmeier-Haack reagent (POCl3/ DMF), followed by cyclization. © 2010, by Walter de Gruyter GmbH & Co. All rights reserved.

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Kumar, R., Prakash, O., & Wadhwa, D. (2010). Beckmann Rearrangement of 2-Hydroxy-5-Methylacetophenone Oxime using Vilsmeier-Haack Reagent (POCl3/ DMF): Synthesis of Some New Heterocycles. Heterocyclic Communications, 16(2–3), 201–205. https://doi.org/10.1515/HC.2010.16.2-3.201

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