Peptide synthesis. Part 6. Protection of the sulphydryl group of cysteine in solid-phase synthesis using Nα-fluorenylmethoxycarbonylamino acids. Linear oxytocin derivatives
- 1 January 1985
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 10,p. 2057-2064
- https://doi.org/10.1039/p19850002057
Abstract
The Nα-fluorenylmethoxycarbonyl derivatives of S-acetamidomethyl-, S-t-butyl-, and S–S–t-butylcysteine have been prepared and used in solid-phase peptide synthesis on polar, poly(dimethylacrylamide) supports. All three derivatives proved suitable as judged by synthesis of the linear oxytocin nonapeptide amide sequence.This publication has 7 references indexed in Scilit:
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