Issue 13, 1978

A mild procedure for solid phase peptide synthesis: use of fluorenylmethoxycarbonylamino-acids

Abstract

Use of base-labile N-fluorenylmethoxycarbonylamino-acids, t-butyl based side chain protecting groups, and a p-alkoxybenzyl ester resin linkage provides a simple, rapid, and exceptionally mild strategy in solid phase peptide synthesis.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 537-539

A mild procedure for solid phase peptide synthesis: use of fluorenylmethoxycarbonylamino-acids

E. Atherton, H. Fox, D. Harkiss, C. J. Logan, R. C. Sheppard and B. J. Williams, J. Chem. Soc., Chem. Commun., 1978, 537 DOI: 10.1039/C39780000537

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