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Selektivita 1,3-dipolárních cykloadicí N-substituovaných karbamoylem stabilizovaných azomethinylidů
Title in English | Selectivity of 1,3-dipolar cycloadditions of N-substituted by carbamoyl stabilized azomethine ylides |
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Authors | |
Year of publication | 2000 |
Type | Article in Periodical |
Magazine / Source | Chemické Listy |
MU Faculty or unit | |
Citation | |
Field | Organic chemistry |
Description | In this paper stereo and regioselectivity of cycloadducts formed during reaction of azomethine ylides generated from quarternary phenanthridinium salts Ia - Id in dry dichloromethane was serched. We found that the generated azomethine ylide reacts with dipolarophiles under formation 1,2,3,12b-tetrahydropyrrolo[1,2-f]phenanthridines. |
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