Publication details
Microwave initiated intramolecular cyclizations of in situ formed azomethine ylide with allylamino group at substituted thiophene
| Authors | |
|---|---|
| Year of publication | 2008 |
| Type | Article in Proceedings |
| Conference | 4th Summer School "Medicinal Chemistry" |
| MU Faculty or unit | |
| Citation | |
| Field | Organic chemistry |
| Keywords | chemistry; microwave; cycloaddition |
| Description | Synthesis of new pyrrolo[3,2-c]pyridine heterocycles by microwave induced cycloaddition reaction. The reaction is proceeding in two subsequent steps. The first is intermolecular reaction of secondary amine with carbonyl moiety forming an intermediate. In the second step the intermediate undergo intramolecular cycloaddition. |
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