An Efficient Procedure for Cleavage of T-Butyl Protected Cysteine in Solid Phase Peptide Synthesis |
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Authors: | He Wang Zhenwei Miao Luhua Lai Xiaojie Xu |
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Institution: | Institute of Physical Chemistry, Peking University , Beijing, 100871, P.R., China |
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Abstract: | In the Fmoc-strategy of solid phase peptide synthesis, 1M trimethylsilyl bromide-thioanisole/trifluoroacetic acid in the presence of 1,2-ethanedithiol as scavenger was found to be an efficient deprotecting procedure for a full cleavage and side chains deprotection of the peptide resin involving t-butyl protected cysteine. In addition, selective deprotection of the peptide resin containing protected cysteine was also described based on this method. |
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Keywords: | Epoxide Aromatic amine Zirconium (IV) chloride |
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