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@ARTICLE{Liu:858485,
      author       = {Liu, Yang and Kurtán, Tibor and Mándi, Attila and Weber,
                      Horst and Wang, Changyun and Hartmann, Rudolf and Lin,
                      Wenhan and Daletos, Georgios and Proksch, Peter},
      title        = {{A} novel 10-membered macrocyclic lactone from the
                      mangrove-derived endophytic fungus {A}nnulohypoxylon sp.},
      journal      = {Tetrahedron letters},
      volume       = {59},
      number       = {7},
      issn         = {0040-4039},
      address      = {Amsterdam [u.a.]},
      publisher    = {Elsevier Science},
      reportid     = {FZJ-2018-07357},
      pages        = {632 - 636},
      year         = {2018},
      abstract     = {A novel 10-membered macrolactone, hypoxylide (1), was
                      isolated from the endophytic fungus Annulohypoxylon sp. that
                      was obtained from the Mangrove plant Rhizophora racemosa.
                      The structure and absolute configuration of 1 were
                      unambiguously elucidated by comprehensive 1D and 2D NMR, as
                      well as by HRESIMS and ECD spectroscopic analyses.
                      Hypoxylide (1) features an unprecedented polyketide skeleton
                      comprised of a trihydroxynaphthalene-dione moiety fused to a
                      decalactone ring. A plausible biosynthetic pathway of this
                      novel metabolite is proposed.},
      cin          = {ICS-6},
      ddc          = {540},
      cid          = {I:(DE-Juel1)ICS-6-20110106},
      pnm          = {551 - Functional Macromolecules and Complexes (POF3-551)},
      pid          = {G:(DE-HGF)POF3-551},
      typ          = {PUB:(DE-HGF)16},
      UT           = {WOS:000424717600012},
      doi          = {10.1016/j.tetlet.2018.01.001},
      url          = {https://juser.fz-juelich.de/record/858485},
}