Reference 6 should be modified as follows.
Combination of silyl carbamate and amino acid fluoride for solid-phase peptide synthesis
β Scribed by Kimitoshi Sakamoto; Yoshiaki Nakahara; Yukishige Ito
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 133 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Diketopiperadine (DKP) formation is an often encountered side reaction in the synthesis of peptide having C-terminal proline ester. A novel strategy for the avoidance of this side reaction was developed, which utilizes Pfp ester of Tsoc-amino acid and Fmoc-amino acid fluoride as the second and the third amino acid, respectively. This strategy was applied to the synthesis of 37-53 fragment of the b-chain of human chorionic gonadotropin (hCG).
π SIMILAR VOLUMES
The solid-phase syntheses of enkephalin and somatostatin analogues with C-terminal OH functions instead of the normal carboxylates are described. The OH function of the N-terminal amino alcohol was acylated with succinic acid and esterified to the solid support. Normal Boc-TFA solid-phase strategy c