✍ Scribed by John Hachmann; Michal Lebl
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Ten different coupling reagents and their combinations were tested in parallel in the synthesis of four model peptide sequences. Significant differences were found between uronium and phosphonium salt‐based reagents and carbodiimide. Diisopropylcarbodiimide was identified as an optimal reagent based on the purity of the product, stability of the reagent, and convenience of handling on plate‐based multiple parallel centrifugation synthesizer. © 2006 Wiley Periodicals, Inc. Biopolymers (Pept Sci) 84: 340–347, 2006
This article was originally published online as an accepted preprint. The “Published Online” date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office at [email protected]
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