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Open Access
A NOVEL SYNTHESIS OF BENZO[g]IMIDAZO[1,2-a]PYRIDINES: THE REACTIVITY OF ARYLIDINE-1H-BENZIMIDAZOLE-2- ACETONITRILE WITH ELECTRON POOR OLEFINS AND DIMETHYLACETYLENE DICARBOXYLATE UNDER MICROWAVE IRRADIATION
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Ramadan Mekheimer,
Published/Copyright:
June 1, 1997
Published Online: 1997-06
©2011 by Walter de Gruyter GmbH & Co.
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Articles in the same Issue
- CONTRIBUTORS TO THIS ISSUE
- Graphical Abstracts
- FUSED PYRAZOLE SYNTHESIS BY N-N BOND FORMATION: THE PYRAZOLO[5,1-b]BENZOTHIAZOLE SYSTEM
- IODINATION OF BENZOCYCLIC AMINES WITH MERCURY(II)OXIDE-IODINE REAGENT
- OXAZEPINES AND THIAZEPINES 35. SYNTHESIS OF TETRACYCLIC BENZODIAZEPINES BY THE REACTION OF 2-AMIN0THI0PHEN0L WITH EXOCYCLIC α,β-EN0NES
- A NOVEL SYNTHESIS OF BENZO[g]IMIDAZO[1,2-a]PYRIDINES: THE REACTIVITY OF ARYLIDINE-1H-BENZIMIDAZOLE-2- ACETONITRILE WITH ELECTRON POOR OLEFINS AND DIMETHYLACETYLENE DICARBOXYLATE UNDER MICROWAVE IRRADIATION
- DEHYDROGENATION BY IODINE/DIMETHYLSULFOXIDE SYSTEM: A GENERAL ROUTE TO SUBSTITUTED CHROMONES AND THIOCHROMONES
- Addition and Cycloaddition Reactions with Pyrazole Blue
- DIASTEREOSELECTIVE PREPARATION AND STRUCTURE OF NOVEL CYCLOPHOSPHAMIDE DERIVATIVES OF AMINO ACIDS
- SYNTHESIS OF SOME NOVEL PYRAZOLINES AS BIOLOGICALLY POTENT AGENTS
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- SYNTHESIS OF ANTHRA[2,3-b]BENZOFURAN DERIVATIVES BY CYCLIZATION OF LACCAIC ACID A DERIVATIVES AND ITS REACTION MECHANISM
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