Synthesis of the originally proposed structures of elatenyne and an enyne from Laurencia majuscula

Sheldrake, Helen M and Jamieson, Craig and Pascu, Sofia I and Burton, Jonathan W (2009) Synthesis of the originally proposed structures of elatenyne and an enyne from Laurencia majuscula. Organic and Biomolecular Chemistry, 7 (2). pp. 238-252. ISSN 1477-0520

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      Abstract

      A bidirectional synthesis of the originally proposed structures for the natural products elatenyne and a chloroenyne from Laurencia majuscula is described along with a reassessment of the structures of the halogenated enynes based upon a C-13 NMR chemical shift/structure correlation.

      ORCID iDs

      Sheldrake, Helen M, Jamieson, Craig ORCID logoORCID: https://orcid.org/0000-0002-6567-8272, Pascu, Sofia I and Burton, Jonathan W;
      • Item type:Article
        ID code:30851
        Dates:
        Date
        Event
        2009
        Published
        20 November 2008
        Published Online
        Keywords:supramolecular host systems, 2-directional chain synthesis, natural product syntheses, fused polycyclic ethers, Chemistry, Biochemistry, Organic Chemistry, Physical and Theoretical Chemistry
        Subjects:Science > Chemistry
        Department:Faculty of Science > Pure and Applied Chemistry
        Depositing user: Pure Administrator
        Date deposited:05 May 2011 16:24
        Last modified:24 Mar 2021 01:22
        URI:https://strathprints.strath.ac.uk/id/eprint/30851
      CORE (COnnecting REpositories)