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  • In the continuation of the already obtained results on intramolecular 1,3-dipolar cycloadditions, the aim of the project is to conclude explanation of the observed stereoselectivity. New structural models in the reaction will be examined. (en)
  • Cílem projektu je vybrat vhodné a dostupné strukturní modely, které by mohly podpořit nebo vyvrátit dosavadní představy o stereochemickém vlivu na výsledek reakcí v mikrovlnách, tyto modely syntetizovat a použít v intramolekulární cykloadiční reakci.
Title
  • Microwave initiated syntheses (en)
  • Mikrovlnami iniciované syntézy
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  • OC08052
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  • microwaves; intramolecular cycloaddition; stereochemistry (en)
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  • o-Allyloxysubstituted naphtalenecarbaldehydes at 200oC underwent Claisen rearrangement,under 140oC with sec.amines afforded in MW azomethine ylides entering intramolecular stereospecific 1,3-dipolar cycloadditions to hexahydrochromeno[4,3-b]pyrroles. (en)
  • o-Allyloxysubstituované naftalenkarbaldehydy,při 200oC podléhaly Claisenovu přesmyku,při tepl.pod 140oC se sekundár.aminy poskytovaly v MW azomethinylidy reag.v intramolekul.stereospecifické 1,3-dipolární cykloadice na hexahydrochromeno[4,3-b]pyrroly. (cs)
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  • microwaves
  • intramolecular cycloaddition
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