Dihydroisocoumarins from fungi: isolation, structure elucidation, circular dichroism and biological activity.

[1]  R. Zain,et al.  A new entry to nucleoside phosphorofluoridate and nucleoside phosphorofluoridothioate diesters , 1996 .

[2]  V. Wray,et al.  Biologically Active Metabolites from Fungi 71); Aposphaerin A and B Two New Chroman-4-ones from Aposphaeria sp , 1996 .

[3]  Peter G. Jones,et al.  Biologically active secondary metabolites of endophytic Pezicula species , 1995 .

[4]  M. Stadler,et al.  Metabolites with nematicidal and antimicrobial activities from the ascomycete Lachnum papyraceum (Karst.) Karst. III. Production of novel isocoumarin derivatives, isolation, and biological activities. , 1995, The Journal of antibiotics.

[5]  M. Stadler,et al.  New metabolites with nematicidal and antimicrobial activities from the ascomycete Lachnum papyraceum (Karst.) Karst. IV. Structural elucidation of novel isocoumarin derivatives. , 1995, The Journal of antibiotics.

[6]  H. Bestmann,et al.  3,4‐Dihydroisocumarine, eine neue Klasse von Spurpheromonen bei Ameisen , 1992 .

[7]  W. Chilton,et al.  Toxins produced by the Dogwood anthracnose fungus discula sp. , 1991 .

[8]  R. Csuk,et al.  Baker's yeast mediated transformations in organic chemistry , 1991 .

[9]  M. Midland Asymmetric reductions with organoborane reagents , 1989 .

[10]  Harry P. Schultz,et al.  An improved synthesis of 6,8-dimethoxy-3-methylisocoumarin, a fungal metabolite precursor , 1989 .

[11]  S. Attah-poku,et al.  The chemistry of the blue stain fungi. Part 3. Some metabolites of Ceratocystisminor (Hedgcock) Hunt , 1987 .

[12]  Takeshi Matsumoto,et al.  Structures and Phytotoxicity of Metabolites from Valsa ceratosperma , 1986 .

[13]  E. Keinan,et al.  Thermostable enzymes in organic synthesis. 2. Asymmetric reduction of ketones with alcohol dehydrogenase from Thermoanaerobium brockii , 1986 .

[14]  P. Ramachandran,et al.  Diisopinocampheylchloroborane, a remarkably efficient chiral reducing agent for aromatic prochiral ketones , 1985 .

[15]  D. C. Aldridge,et al.  Fungal metabolites II , 1983 .

[16]  Richard J. Cole,et al.  Handbook of toxic fungal metabolites , 1981 .

[17]  O. Gottlieb,et al.  Pterocarpans from Swartzia laevicarpa , 1980 .

[18]  Albert Kollmann,et al.  Dihydroisocoumarines et acide mycophenolique du milieu de culture du champignon phytopathogene septoria nodorum , 1980 .

[19]  L. Merlini,et al.  Metabolites of Cercospora. Taiwapyrone, an α-pyrone of unusual structure from Cercospora taiwanensis , 1976 .

[20]  U. L. Diener,et al.  Mellein and 4-hydroxymellein production by Aspergillus ochraceus Wilhelm. , 1972, Applied microbiology.

[21]  G. Snatzke,et al.  Synthese de methyl-tetralones-1 et de methyl-tetralines optiquement actives , 1971 .

[22]  G. Snatzke,et al.  Circulardichroismus—XL : Chiroptische eigenschaften von aminoindanolen und verwandten verbindungen☆ , 1970 .

[23]  H. Takamatsu,et al.  Studies on the Compounds Produced by Molds , 1970 .

[24]  L. Mitscher,et al.  Dihydroisocoumarins from a Sporormia fungus , 1968 .