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.

      Creators(s): 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
      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:26 Jan 2021 02:24
      URI:https://strathprints.strath.ac.uk/id/eprint/30851
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