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Monitoring solution-phase combinatorial library synthesis by capillary electrophoresis

✍ Scribed by Hans J. Gaus; Pei-Pei Kung; Doug Brooks; P. Dan Cook; Lendell L. Cummins


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
165 KB
Volume
61
Category
Article
ISSN
0006-3592

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✦ Synopsis


Capillary electrophoresis has been applied to monitor model reactions in solution-phase combinatorial chemistry. In particular, the simultaneous alkylation reactions of secondary amines with a series of benzyl halides has been investigated. Reactant and product concentrations were monitored using capillary electrophoresis in a nonaqueous buffer system. The simplified sample preparation was a key feature making this an attractive method of analysis. The results demonstrate that capillary electrophoresis is a useful tool for monitoring reactions to determine initial rates, rate constants, and extinction correlation coefficients for quantitative analysis in combinatorial chemistry, and is a broadly applicable technique for the analysis of a variety of organic and bioorganic transformations.


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A symmetric diketopiperazine scaffold 2 has been prepared in a very simple two-step procedure from l-aspartic acid dimethyl ester. This product (a tetracarboxylic acid equally protected at the two symmetric positions) has been employed as a template for the synthesis of mixed amide libraries in the