ARTICLE;
CONTROLLED STUDY;
DRUG ACETYLATION;
DRUG IDENTIFICATION;
DRUG ISOLATION;
DRUG STRUCTURE;
ENDOPHYTE;
FUNGUS CULTURE;
METHYLATION;
NONHUMAN;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
SCYTALIDIUM;
SPECIES DIFFERENCE;
THIN LAYER CHROMATOGRAPHY;
Metabolites produced by the Scleroderris canker fungus, Gremmeniella abietina
W.A. Ayer, Y. Hoyano, M.S. Pedras and I. van Altena (1986). Metabolites produced by the Scleroderris canker fungus, Gremmeniella abietina. Part 1. Can. J. Chem., 64, 1585-1589.
(1986)Can. J. Chem., vol.64, Issue.PART 1, pp. 1585-1589
Structure and absolute configuration of an atrovenetin-like metabolite from Aspergillus silvaticus
K. Homma, K. Fukuyama, Y. Katsube, Y. Kimura and T. Hamasaki (1980). Structure and absolute configuration of an atrovenetin-like metabolite from Aspergillus silvaticus, Agric. Biol. Chem., 44, 1333-1337.
Cercophorins A-C: Novel antifungal and cytotoxic metabolites from the coprophilous fungus Cercophora areolata
A.C. Whyte and J.B. Gloer (1996). Cercophorins A-C: Novel antifungal and cytotoxic metabolites from the coprophilous fungus Cercophora areolata. J. Nat. Prod., 59, 765-769.
4-Acetyl-6.8-dihydroxy-5-methyl-2-benzopyran-1-one, a metabolite of Aspergillus viridinutans
D.C. Aldridge, J.F. Grove and W.B. Turner (1966). 4-Acetyl-6.8-dihydroxy-5-methyl-2-benzopyran-1-one, a metabolite of Aspergillus viridinutans. J. Chem. Soc. (C), 126-129.
Metabolites from Fungi 15. New isocoumarins from an endophytic fungus isolated from the Canadian thistle Cirsium arvense
K. Krohn, U. Flörke, M.S. Rao, K. Steingröver, H.-J. Aust, S. Draeger and B. Schulz (2001). Metabolites from Fungi 15. New isocoumarins from an endophytic fungus isolated from the Canadian thistle Cirsium arvense. Nat. Prod. Lett., 15, 353-361.
Sescandelin, a new root promoting substance produced by the fungus Sesquicillium candelabrum
Y. Kimura, H. Nakajima and T. Hamasaki (1990). Sescandelin, a new root promoting substance produced by the fungus Sesquicillium candelabrum. Agric. Biol. Chem., 54, 2477-2479.
Synthesis of 4-acetylisocoumarin: First total synthesis of AGI-7 and sescandelin
S. Kim, G.-j. Fan, J. Lee, J.J. Lee and D. Kim (2002). Synthesis of 4-acetylisocoumarin: first total synthesis of AGI-7 and sescandelin. J. Org. Chem., 67, 3127-3130.
7aH-Cyclopent[b]pyran-7-one durch Ringtransformation von 2,4,6-Triaryl-pyryliumsalzen mit acyclischen 1,2-Diketonen
T. Zimmermann, G.W. Fischer and L. Kutschabsky (1989). 7aH-Cyclopent[b]pyran-7-one durch Ringtransformation von 2,4,6-Triaryl-pyryliumsalzen mit acyclischen 1,2-Diketonen. J. prakt. Chem., 331, 293-305.
Synthesis and oral antifungal activity of novel azolylpropanolones and related compounds
M. Ogata, H. Matsumoto, K. Takahashi, S. Shimizu, S. Kida, A. Murabayashi, M. Shiro and K. Tawara (1987). Synthesis and oral antifungal activity of novel azolylpropanolones and related compounds. J. Med. Chem., 30, 1054-1068.