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Highly regioselective 1,3-dipolar cycloaddition of diphenylnitrilimine to Sc3N@Ih-C80 affording a very stable, unprecedented pyrazole-ring fused derivative of endohedral metallofullerenes
- Source :
- Chem. Commun.. 50:12710-12713
- Publication Year :
- 2014
- Publisher :
- Royal Society of Chemistry (RSC), 2014.
-
Abstract
- Formation of a very stable, unprecedented pyrazole-ring fused derivative of endohedral metallofullerenes was achieved by the first 1,3-dipolar cycloaddition reaction of Sc3N@C80 with diphenylnitrilimine in a highly regioselective manner.
- Subjects :
- Cycloaddition Reaction
Chemistry
Stereochemistry
Molecular Conformation
Metals and Alloys
Regioselectivity
Stereoisomerism
General Chemistry
Pyrazole
Crystallography, X-Ray
Ring (chemistry)
Catalysis
Cycloaddition
Surfaces, Coatings and Films
Electronic, Optical and Magnetic Materials
chemistry.chemical_compound
1,3-Dipolar cycloaddition
Materials Chemistry
Ceramics and Composites
Pyrazoles
Fullerenes
Imines
Scandium
Derivative (chemistry)
Subjects
Details
- ISSN :
- 1364548X and 13597345
- Volume :
- 50
- Database :
- OpenAIRE
- Journal :
- Chem. Commun.
- Accession number :
- edsair.doi.dedup.....1499d318e15670ae33bbe69de3c1980b