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A new reagent for the cleavage of fully protected peptides synthesised on 2-chlorotrityl chloride resin

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Bollhagen,  Ralf
Department of Biophysical Chemistry, Max Planck Institute of Biophysics, Max Planck Society;

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Schmiedberger,  Monika
Department of Biophysical Chemistry, Max Planck Institute of Biophysics, Max Planck Society;

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Grell,  Ernst
Department of Biophysical Chemistry, Max Planck Institute of Biophysics, Max Planck Society;

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Citation

Bollhagen, R., Schmiedberger, M., Barlos, K., & Grell, E. (1994). A new reagent for the cleavage of fully protected peptides synthesised on 2-chlorotrityl chloride resin. Journal of the Chemical Society, Chemical Communications, 22, 2559-2560. doi:10.1039/C39940002559.


Cite as: http://hdl.handle.net/21.11116/0000-0008-01F0-7
Abstract
A mixture of hexafluoroisopropanol–dichloromethane (1:4 v/v) acts as a fast, effective and convenient reagent for cleaving protected peptide fragments with a minimal amount of racemization from 2-chlorotrityl chloride resin.