Issue 21, 1999

Hypophosphite mediated carbon–carbon bond formation: total synthesis of epialboatrin and structural revision of alboatrin

Abstract

1-Ethylpiperidine hypophosphite (1-EPHP) has been used in the key radical-cyclisation step in a 6-step synthesis of the phytotoxic metabolite alboatrin and its epimer from orcinol. The synthesis demonstrates that the stereochemistry of the structure initially proposed for alboatrin requires revision.

Supplementary files

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1999, 3071-3073

Hypophosphite mediated carbon–carbon bond formation: total synthesis of epialboatrin and structural revision of alboatrin

S. R. Graham, J. A. Murphy and A. R. Kennedy, J. Chem. Soc., Perkin Trans. 1, 1999, 3071 DOI: 10.1039/A907032J

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