Selektivita 1,3-dipolárních cykloadicí N-substituovaných karbamoylem stabilizovaných azomethinylidů

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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.
Related projects:	Structure and character of bonding, properties and analysis of synthetic and natural molecular ensembles