Issue 32, 2011

Synthesis of a cyclic peptide/protein using the NEXT-A reaction followed by cyclization

Abstract

By using the NEXT-A reaction, we introduced a non-natural amino acid at the N-terminus of a peptide/protein that contained a cysteine unit. The side chain of the introduced amino acid spontaneously reacted with the cysteine to afford a cyclic peptide/protein.

Graphical abstract: Synthesis of a cyclic peptide/protein using the NEXT-A reaction followed by cyclization

Supplementary files

Article information

Article type
Communication
Submitted
16 Apr 2011
Accepted
23 Jun 2011
First published
07 Jul 2011

Chem. Commun., 2011,47, 9116-9118

Synthesis of a cyclic peptide/protein using the NEXT-A reaction followed by cyclization

T. Hamamoto, M. Sisido, T. Ohtsuki and M. Taki, Chem. Commun., 2011, 47, 9116 DOI: 10.1039/C1CC12196K

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.

Social activity

Spotlight

Advertisements