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Enantioselective Cycloaddition of Münchnones onto [60]Fullerene: Organocatalysis versus Metal Catalysis
Author(s) -
Juan MarcoMartínez,
Silvia Reboredo,
Marta Izquierdo,
Vanesa Marcos,
Juan Luis López,
Salvatore Filippone,
Nazario Martı́n
Publication year - 2014
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja500071k
Subject(s) - enantioselective synthesis , chemistry , cycloaddition , fullerene , organocatalysis , catalysis , enantiomer , organic chemistry , enantiomeric excess , combinatorial chemistry , surface modification
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.

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