Racemization-Free synthesis of c-terminal cysteine-peptide using 2-chlorotrityl resin

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Abstract

We investigated the effects of bases, resins, and S-protecting groups on the extent of racemization at the C-terminal cysteine during Fmoc-based(Fmoc=fluoren-9-yl-methoxy-carbonyl) solid phase peptide synthesis. The use of 2-chlorotrityl resin was most effective in suppressing the racemization caused by the base treatment for Fmoc-cleavage. Somatostatin was successfully synthesized with practically no racemization using 2-chlorotrityl resin by Fmoc-chemistry. © 1994, The Pharmaceutical Society of Japan. All rights reserved.

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Fujiwara, Y., Akaji, K., & Kiso, Y. (1994). Racemization-Free synthesis of c-terminal cysteine-peptide using 2-chlorotrityl resin. Chemical and Pharmaceutical Bulletin, 42(3), 724–726. https://doi.org/10.1248/cpb.42.724

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