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

J Am Chem Soc

Departamento de Química Orgánica I, Facultad de Química, Universidad Complutense , E-28040 Madrid, Spain.

Published: February 2014

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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3954715PMC
http://dx.doi.org/10.1021/ja500071kDOI Listing

Publication Analysis

Top Keywords

enantioselective cycloaddition
8
cycloaddition münchnones
8
münchnones [60]fullerene
4
[60]fullerene organocatalysis
4
organocatalysis versus
4
versus metal
4
metal catalysis
4
catalysis novel
4
novel chiral
4
chiral catalytic
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!