Publication details
Microwave initiated in situ formed azomethine ylides from variously substituted allyloxy naphtahalene carbaldehydes and secondary amines in intramolecular 1,3-dipolar cycloadditions
| Authors | |
|---|---|
| Year of publication | 2009 |
| Type | Article in Proceedings |
| Conference | Book of Abstracts COST Action D32 Final Meeting |
| MU Faculty or unit | |
| Citation | |
| Field | Organic chemistry |
| Keywords | microwave; cycloaddition; stereochemistry |
| Description | Application of microwave in intramolecular 1,3-dipolar cycloaddition and stereospecifity of the reactions. Reactions were ivestigated at variously substituted naphtalene skeletons bearing in alfa, beta positions aldehyde and allyloxy groups with secondary amines. |
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