Literature DB >> 18007493

Quantum chemical and experimental studies on the mechanism of alkylation of beta-dicarbonyl compounds. The synthesis of five and six membered heterocyclic spiro derivatives.

Nurettin Sadikov1, Sahin Nasibov, Cemil Oğretir, Halil Berber, Ali Hüseyinli.   

Abstract

The alkylation of beta-dicarbonyl compounds in a K2CO3/DMSO system was found to afford O- and C-alkylated derivatives, depending on the type of the beta-dicarbonyl compound involved. The alkyl derivatives obtained were used in the synthesis of some new spiro barbituric acid derivatives. Quantum chemical calculations were carried out to elucidate the reaction mechanisms for some typical synthesis.

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Year:  2004        PMID: 18007493      PMCID: PMC6147278          DOI: 10.3390/91100922

Source DB:  PubMed          Journal:  Molecules        ISSN: 1420-3049            Impact factor:   4.411


  1 in total

1.  Intramolecular Pauson-Khand reactions of methylenecyclopropane and bicyclopropylidene derivatives as an approach to spiro(cyclopropanebicyclo[n.3.0]alkenones).

Authors:  Armin de Meijere; Heike Becker; Andreas Stolle; Sergei I Kozhushkov; M Teresa Bes; Jacques Salaün; Mathias Noltemeyer
Journal:  Chemistry       Date:  2005-04-08       Impact factor: 5.236

  1 in total

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