Synthesis of novel derivatives of pyridine-2,6-dicarboxylic acid

Synthetic Communications

Volumn 36, Issue 14, 2006, Pages 2027-2034

  Tang, Rui ren ^a   Zhao, Qiang ^a   Yan, Zi er ^a   Luo, Yi ming ^a  

^a CENTRAL SOUTH UNIVERSITY   (China)

Author keywords

Ligands; Pyridine 2,6 dicarboxylic; Synthesis

Indexed keywords

DICARBOXYLIC ACID; PRIDINE 2,6 DICARBOXYLIC ACID; UNCLASSIFIED DRUG;

AMINOLYSIS; ANALYTIC METHOD; ARTICLE; COMPLEX FORMATION; DERIVATIZATION; LIGAND BINDING; NUCLEAR MAGNETIC RESONANCE; RADIOIMMUNOASSAY; SYNTHESIS; THIN LAYER CHROMATOGRAPHY;

EID: 33745290655     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910600634381     Document Type: Article

References (9)

1. Yin, X. H.; Tan, M. Y. Synthesis of novel multifunctional pyridine-2-6-dicarboxylic acid derivatives. Synth. Commun. 2003, 33 (7), 1113-1119.
2. Muller, G.; Schmidt, B.; Jiricek, J.; Hopfgartner, G.; Riehl, J. P.; Buenzli, J.-C. G. Lanthanide triple helical complexes with a chiral ligand derived from 2,6-pyridine-carboxylic acid. J. Chem. Soc., Dalton Trans. 2001, 18, 2655-2662.
3. (a) Muller, W. G. Advances in Microbial Physiology; Academic Press: London and New York, 1967; Vol. 1, 113-262;
4. (b) Highfield, J. A.; Mehta, L. K.; Parrick, J.; Wardman, P. Synthesis, hydroxyl radical production and cytotoxicity of analogues of bleomycin. Bioorg. Med. Chem. 2000, 8 (5), 1065-1073.
5. Lamture, J. B.; Zhou, Z. H.; Kumar, A. S.; Wensel, T. G. Luminescent properties of terbium complexes with 4-substituted dipicolinic acid analogues. Inorg. Chem. 1995, 34, 864-869.
6. Buratti, W.; Gardini, G. P.; Minisci, F. Nucleophilic character of alkyl radicals. Tetrahedron 1971, 27 (15), 3655-3668.
7. Shelkov, R.; Melman, A. Free-radical approach to 4-substituted dipicolinates. Eur. J. Org. Chem. 2005, (7), 1397-1401.
8. Claramunt, R. M.; Hernandez, H.; Elguero, J.; Julia, S. Bull. Soc. Chim. Fr. 1983, (1-2), 5-10.
9. Biniecki, S.; Modrzejewska, W.; Rogla-Zawadzka, A. Acta Poloniae Pharmaceutica 1985, 42 (1), 1-3.