In order to minimise the formation of the pyrophosphate derivative of the target peptide when side-chainunprotected phopshotyrosine is used in solid-phase peptide synthesis, this building block can be incorporated using benzotriazolyloxy-tris-(dimethylamino)phosphonium hexafluorophosphate/1-hydroxyb
✦ LIBER ✦
Potential pyrophosphate formation upon use ofNα-Fmoc-Tyr(PO3H2)-OH in solid-phase peptide synthesis
✍ Scribed by Carlos García-Echeverría
- Publisher
- Springer Netherlands
- Year
- 1995
- Tongue
- English
- Weight
- 361 KB
- Volume
- 2
- Category
- Article
- ISSN
- 1573-3149
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✦ Synopsis
A series of peptides related to some of the autophosphorylation sites of the epidermal growth factor receptor has been synthesized on solid phase, using side-chain-unprotected phosphotyrosine. Although the desired peptides could be obtained, this approach was not entirely satisfactory due to a side reaction that gave the pyrophosphate derivative of the target peptide. Under identical coupling conditions, the extension of this side reaction appears to be sequence dependent.
📜 SIMILAR VOLUMES
Evaluation of coupling conditions for th
✍
Carlos García-Echeverría
📂
Article
📅
1996
🏛
Springer Netherlands
🌐
English
⚖ 305 KB