Issue 16, 2011

“Inosaminoacids”: novel inositol–amino acid hybrid structures accessed by microbial areneoxidation

Abstract

Microbial 1,2-dihydroxylation of sodium benzoate permits the rapid construction of novel inositolamino acid hybrid structures. Both β- and γ-amino acids are accessible by means of an acylnitroso Diels–Alder cycloaddition.

Graphical abstract: “Inosaminoacids”: novel inositol–amino acid hybrid structures accessed by microbial arene oxidation

Supplementary files

Article information

Article type
Communication
Submitted
01 Feb 2011
Accepted
01 Mar 2011
First published
15 Mar 2011

Chem. Commun., 2011,47, 4799-4801

“Inosaminoacids”: novel inositolamino acid hybrid structures accessed by microbial arene oxidation

S. Pilgrim, G. Kociok-Köhn, M. D. Lloyd and S. E. Lewis, Chem. Commun., 2011, 47, 4799 DOI: 10.1039/C1CC10643K

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