1,3-DIPOLAR CYCLOADDITION REACTION OF [60]FULLERENE AND IMINES OF ALPHA-AMINO-ACID ESTERS - FORMATION OF FULLERENE-FUSED PROLINE DERIVATIVES

Authors
SHU LH WANG GW WU SH WU HM LAO XF
Citation
Lh. Shu et al., 1,3-DIPOLAR CYCLOADDITION REACTION OF [60]FULLERENE AND IMINES OF ALPHA-AMINO-ACID ESTERS - FORMATION OF FULLERENE-FUSED PROLINE DERIVATIVES, Tetrahedron letters, 36(22), 1995, pp. 3871-3874
Citations number
9
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
36
Issue
22
Year of publication
1995
Pages
3871 - 3874
Database
ISI
SICI code
0040-4039(1995)36:22<3871:1CRO[A>2.0.ZU;2-8
Abstract
[60]Fullerene reacts thermally with imines of a-amino acid esters to g ive two Isomers of fullerene-fused proline derivatives via a process o f 1,3-dipolar cycloaddition. The products were characterized by FT-IR, W-Vis, H-1-NMR, H-1-NOESY and C-13-NMR spectroscopic techniques.