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

Helen M Sheldrake, Craig Jamieson, Sofia I Pascu, Jonathan W Burton

Research output: Contribution to journalArticle

28 Citations (Scopus)

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.
LanguageEnglish
Pages238-252
Number of pages15
JournalOrganic and Biomolecular Chemistry
Volume7
Issue number2
Early online date20 Nov 2008
DOIs
Publication statusPublished - 2009

Fingerprint

Laurencia
Chemical shift
Biological Products
chemical equilibrium
Nuclear magnetic resonance
nuclear magnetic resonance
synthesis
products
elatenyne

Keywords

  • supramolecular host systems
  • 2-directional chain synthesis
  • natural product syntheses
  • fused polycyclic ethers

Cite this

Sheldrake, Helen M ; Jamieson, Craig ; Pascu, Sofia I ; Burton, Jonathan W. / Synthesis of the originally proposed structures of elatenyne and an enyne from Laurencia majuscula. In: Organic and Biomolecular Chemistry. 2009 ; Vol. 7, No. 2. pp. 238-252.
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Synthesis of the originally proposed structures of elatenyne and an enyne from Laurencia majuscula. / Sheldrake, Helen M; Jamieson, Craig; Pascu, Sofia I; Burton, Jonathan W.

In: Organic and Biomolecular Chemistry, Vol. 7, No. 2, 2009, p. 238-252.

Research output: Contribution to journalArticle

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KW - 2-directional chain synthesis

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KW - fused polycyclic ethers

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