A New Highly Versatile Handle for Chemistry on a Solid Support: The Pipecolic Linker |
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Authors: | Paweł Zajdel Dr. Gaël Nomezine Nicolas Masurier Dr. Muriel Amblard Dr. Maciej Pawłowski Prof. Jean Martinez Prof. Gilles Subra Dr. |
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Affiliation: | 1. Institut des Biomolécules Max Mousseron IBMM, UMR CNRS 5247, 15 avenue Charles Flahault, 34000 Montpellier (France), Fax: (+33)?467548654;2. Department of Medicinal Chemistry, Jagiellonian University Medical College, 9 Medyczna Street, 30‐688 Kraków (Poland) |
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Abstract: | The design, synthesis, and potential application of the pipecolic linker is presented. This new versatile handle can immobilize primary, secondary, and aromatic amines, as well as alcohols, phenols, and hydrazides, on a solid support. Compared with other linkers, the anchoring step is easy and efficient. The release of final products from the resin proceeds upon acidic treatment with high purities. The pipecolic linker offers the promise of being using in peptide chemistry to produce peptides modified at the N and C terminus, peptidomimetics, as well as small organic molecules. |
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Keywords: | amino acids C‐terminal modification hydrazides pipecolic linkers solid‐phase synthesis |
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