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Issue 16, 2011
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“Inosaminoacids”: novel inositol–amino acid hybrid structures accessed by microbial areneoxidation

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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

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Supplementary files

Article information


Submitted
01 Feb 2011
Accepted
01 Mar 2011
First published
15 Mar 2011

Chem. Commun., 2011,47, 4799-4801
Article type
Communication

“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

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