Publication details
1,3-Dipolar Cycloadditions of Phenanthridinium-Based Azomethine Ylides
| Authors | |
|---|---|
| Year of publication | 1994 |
| Type | Article in Periodical |
| Magazine / Source | Bulletin des Sociétés Chimiques Belges |
| MU Faculty or unit | |
| Citation | |
| Field | Organic chemistry |
| Keywords | Dipolar Cycloadditions; Phenanthridinium; Azomethine Ylides |
| Description | 1,3-Dipolar Cycloadditions; Phenanthridinium; Azomethine Ylides. Azomethine ylides generated from 5-(alkoxycarbonylmethyl)phenanthridinium cations were studied in 1,3-dipolar cycloadditions with dimethyl maleate and dimethyl fumarate as dipolarophiles. The cycloadducts with the pyrrolidino[1,2-f]phenanthridine skeleton easily underwent dehydrogenation. The structure of products was determined by X-ray, NMR and MS. |