Issue 0, 1985

Peptide synthesis. Part 6. Protection of the sulphydryl group of cysteine in solid-phase synthesis using Nα-fluorenylmethoxycarbonylamino acids. Linear oxytocin derivatives

Abstract

The Nα-fluorenylmethoxycarbonyl derivatives of S-acetamidomethyl-, S-t-butyl-, and SS–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.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1985, 2057-2064

Peptide synthesis. Part 6. Protection of the sulphydryl group of cysteine in solid-phase synthesis using Nα-fluorenylmethoxycarbonylamino acids. Linear oxytocin derivatives

E. Atherton, M. Pinori and R. C. Sheppard, J. Chem. Soc., Perkin Trans. 1, 1985, 2057 DOI: 10.1039/P19850002057

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements