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Issue 31, 2017
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Stereoselective synthesis of the viridiofungin analogue NA808 from a chiral tetrahydrofuran-carboxylic acid

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Abstract

The viridiofungin analogue NA808 was synthesized by the stereoselective Ireland–Claisen rearrangement of dienylmethyl ester, regioselective bromolactonization of β-divinylpropanoic acid and retro-bromolactonization.

Graphical abstract: Stereoselective synthesis of the viridiofungin analogue NA808 from a chiral tetrahydrofuran-carboxylic acid

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Publication details

The article was received on 03 Jul 2017, accepted on 24 Jul 2017 and first published on 24 Jul 2017


Article type: Paper
DOI: 10.1039/C7OB01608E
Citation: Org. Biomol. Chem., 2017,15, 6632-6639
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    Stereoselective synthesis of the viridiofungin analogue NA808 from a chiral tetrahydrofuran-carboxylic acid

    M. Murakata and T. Ikeda, Org. Biomol. Chem., 2017, 15, 6632
    DOI: 10.1039/C7OB01608E

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