Enantioselective cycloaddition of münchnones onto [60]fullerene: organocatalysis versus metal catalysis

Novel chiral catalytic systems based on both organic compounds and metal salts have been developed for the enantioselective [3 + 2] cycloaddition of münchnones onto fullerenes and olefins. These two different approaches proved to be efficient and complementary in the synthesis of optically active py...

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Veröffentlicht in:Journal of the American Chemical Society 2014-02, Vol.136 (7), p.2897-2904
Hauptverfasser: Marco-Martínez, Juan, Reboredo, Silvia, Izquierdo, Marta, Marcos, Vanesa, López, Juan Luis, Filippone, Salvatore, Martín, Nazario
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Sprache:eng
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Zusammenfassung:Novel chiral catalytic systems based on both organic compounds and metal salts have been developed for the enantioselective [3 + 2] cycloaddition of münchnones onto fullerenes and olefins. These two different approaches proved to be efficient and complementary in the synthesis of optically active pyrrolino[3,4:1,2][60]fullerenes with high levels of enantiomeric excess and moderate to good conversions. Further functionalization of the pyrrolinofullerene carboxylic acid derivatives has been carried out by esterification and amidation reactions.
ISSN:0002-7863
1520-5126
1520-5126
DOI:10.1021/ja500071k