Stereoselective synthesis of the viridiofungin analogue NA808 from a chiral tetrahydrofuran-carboxylic acidElectronic supplementary information (ESI) available. See DOI: 10.1039/c7ob01608e
The viridiofungin analogue NA808 was synthesized by the stereoselective Ireland-Claisen rearrangement of dienylmethyl ester, regioselective bromolactonization of β-divinylpropanoic acid and retro-bromolactonization. The viridiofungin analogue NA808 was synthesized by the stereoselective Ireland-Clai...
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| Format: | Artikel |
| Sprache: | eng |
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| Zusammenfassung: | The viridiofungin analogue NA808 was synthesized by the stereoselective Ireland-Claisen rearrangement of dienylmethyl ester, regioselective bromolactonization of β-divinylpropanoic acid and retro-bromolactonization.
The viridiofungin analogue NA808 was synthesized by the stereoselective Ireland-Claisen rearrangement of dienylmethyl ester, regioselective bromolactonization of β-divinylpropanoic acid and retro-bromolactonization. |
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| ISSN: | 1477-0520 1477-0539 |
| DOI: | 10.1039/c7ob01608e |