Publication details

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
Authors

POSPÍŠIL Jiří TRÁVNÍČEK Martin POTÁČEK Milan

Year of publication 2000
Type Article in Periodical
Magazine / Source Chemické Listy
MU Faculty or unit

Faculty of Science

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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