HPLC with amperometric detection for the determination of pesticides of high polarity

A relatively simple procedure is described for the selective and highly sensitive determination of amitrole (3-amino-1,2,4-triazole) by ionpair HPLC with amperometric detection. The separation was achieved on a polar CN-column using hexane, propanol, water (62:36:2) with LiClO₄ (2.5 g·l^–1) and trichloroacetic acid (2 g·l^–1) as electrolytes. The determination range lies between 500 pg and 500 ng and the limit of detection was found to be 200 pg (s.d.: 11%; N=9). The minimum detectability for the alternative UV-monitoring was 2.5 ng. The developed method may be helpful in production and quality control and for the selective determination of amitrole in commercial formulations.     

Complex polymer architectures through dimethoxymethyl 1,1‐diphenylethylene derivatives

The reactions of polystyryllithium and potassium on dimethoxymethyl 1,1‐diphenylethylene derivatives were studied in different solvents. In a polar medium, A₃ and A₆ star types were formed according to the stoichiometry, whereas in a nonpolar medium, hyperbranched structures were synthesized. Extensions of an already proposed mechanism in polar and nonpolar media were examined. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 3329–3335, 2003     

Novel antibiotics: second generation macrocyclic peptides designed to trap Holliday junctions

Described are the syntheses of 15 macrocyclic peptides designed to trap Holliday junctions (HJs) in bacteria during site-specific and homologous recombination. This leads to inhibiting bacterial growth. These second generation macrocycles were based on the C-2 symmetrical HJ. They were synthesized using a strategy that permits elucidation of the amino acid role in binding HJs. The syntheses of these macrocycles are an important step in the development of a new class of antibiotics.     

2,4,6‐Trifluoropyrimidine. Reactions with nitrogen nucleophiles

In a continuation of our studies involving the nucleophilic displacement of one of the chlorines from 2,4,6‐trichloropyrimidine, we now report the initial displacement of one of the fluorine atoms from 2,4,6‐trifluoropyrimidine using both aliphatic and aromatic amines. The monosubstitution products favor 2‐substitution with ammonia and ethanolamine while aniline gave the 4‐substituted derivative as the preferred product.