Issue 45, 2009
From the journal:

Chemical Communications

Solid-phase synthesis of protected α-amino phosphonic acid oligomers†‡

Yoshitaka Ishibashia  and  Masato Kitamura*a  

* Corresponding authors

a Research Center for Materials Science and the Department of Chemistry, Nagoya University, Chikusa, Japan
E-mail: kitamura@os.rcms.nagoya-u.ac.jp
Fax: +81 52-789-2958

Abstract

By establishing both a highly efficient phosphonamidate formation and a RuCp-catalyzed cleavage of an allyl linker, the solid-phase synthesis of Fmoc-(GlyP(OBn))6-OH/DIEA, a protected form of a new type of unnatural peptide α-amino phosphonic acid oligomer (APO), has been realized.

Graphical abstract: Solid-phase synthesis of protected α-amino phosphonic acid oligomers

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B912231A
Article type
Communication
Submitted
22 jun. 2009
Accepted
30 sep. 2009
First published
14 oct. 2009

Chem. Commun., 2009, 6985-6987

Permissions

Request permissions

Solid-phase synthesis of protected α-amino phosphonic acid oligomers

Y. Ishibashi and M. Kitamura, Chem. Commun., 2009, 6985 DOI: 10.1039/B912231A

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