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Issue 16, 2011
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“Inosaminoacids”: novel inositolamino acid hybrid structures accessed by microbial arene oxidation

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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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Publication details

The article was received on 01 Feb 2011, accepted on 01 Mar 2011 and first published on 15 Mar 2011


Article type: Communication
DOI: 10.1039/C1CC10643K
Citation: Chem. Commun., 2011,47, 4799-4801
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    “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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