Issue 11, 1994

Synthesis of methyl (1R,2S)-2-[(1′Z,4′Z,7′Z)-hexadeca-1′,4′,7′-trienyl]cyclopropanecarboxylate: a potential inhibitor of the enzyme 5-lipoxygenase

Abstract

We describe the synthesis of a novel cyclopropyl analogue of arachidonic acid via a convergent synthesis that employed methyl (1R,2S)-2-formylcyclopropanecarboxylate in conjunction with the ylide from (3Z,6Z)-pentadeca-3,6-dienyl(triphenyl)phosphonium iodide. This compound was designed to inhibit the enzyme 5-lipoxygenase after reaction to form a putative α-cyclopropylmethylene radical.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1994, 1503-1508

Synthesis of methyl (1R,2S)-2-[(1′Z,4′Z,7′Z)-hexadeca-1′,4′,7′-trienyl]cyclopropanecarboxylate: a potential inhibitor of the enzyme 5-lipoxygenase

P. I. Butler, T. Clarke, C. Dell and J. Mann, J. Chem. Soc., Perkin Trans. 1, 1994, 1503 DOI: 10.1039/P19940001503

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