Total Synthesis of (+)-Agelasidine C, a Physiologically Active Marine Diterpenoid with Hypotaurocyamine Group

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<jats:title>Abstract</jats:title> <jats:p>The introduction of hypotaurocyamine unit to terpenic chain was examined using farnesyl bromide as a model compound and this was feasible by chemoselective oxidation of the derived sulfide by peracid. By the application of the method thus established, a total synthesis of agelasidine C has been accomplished.</jats:p>

Journal

  • Chemistry Letters

    Chemistry Letters 18 (10), 1813-1814, 1989-10-01

    Oxford University Press (OUP)

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