Publication details
Microwave - Assisted Synthesis of Substituted Hexahydro-pyrrolo[3,2-c]quinolines
| Authors | |
|---|---|
| Year of publication | 2007 |
| Type | Article in Periodical |
| Magazine / Source | Molecules |
| MU Faculty or unit | |
| Citation | |
| Field | Organic chemistry |
| Keywords | Azomethine ylide; intramolecular 1/3-dipolar cycloaddition; microwave - assisted synthesis; hexahydro-1H-pyrrolo[3/2-c]quinoline |
| Description | New compounds with the ethyl hexahydro-1H-pyrrolo[3,2-c]quinoline-2-carboxylate skeleton were prepared by microwave-assisted intramolecular 1,3-dipolar cycloaddition reactions. The reactions were carried out under solvent-free conditions and compared with the same reaction in the presence of a solvent and a catalyst. Steric effects on the selectivity of the reaction were noted and evaluated. |
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