Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5271568 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
Chemical investigation of an endophytic fungus, Pestalotiopsis theae, isolated from the leaves of Turraeanthus longipes (Meliaceae) collected in Cameroon, resulted in the isolation of six new epoxyquinols, cytosporins F-K (2-7), together with the known cytosporin D (1). The structures of the new compounds were unambiguously determined by analysis of the 1D, 2D NMR, and HRMS spectra. Cytosporins G-K (3-7) are the first cytosporins with a hydroxyl substituted C7 side chain, while cytosporins F-I (2-5) contain a 13-acetoxyl group that was not reported previously. A plausible biosynthetic pathway for the cytosporin derivatives is proposed.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Sergi Herve Akone, Mustapha El Amrani, Wenhan Lin, Daowan Lai, Peter Proksch,