• Applied Biological Chemistry
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• v.37 no.5
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• pp.402-408
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• 1994

For the examination of the role of monocerin(1) on the biological activity, (8S, 9S, 11R)-(-)-monocerin(20) and (9S, 11R)-(+)-fusarentin 4, 5-dimethyl ether(19) were synthesized by a condensation of the benzylic anion of ethyl 2, 3, 4-trimethoxy-6-methylbenzoate(16) with modifyed (R)-ethyl 3-hydroxyhexanoate (9). In a key step, bioreduction with active dried baker's yeast in organic solvent system was employed to get a chiral aldehyde 12. Their phytotoxic activities were tested on rice seedlings and lettuce seeds.

• Journal of Applied Biological Chemistry
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• v.42 no.1
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• pp.45-47
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• 1999

Two phytotoxic compounds were isolated from a culture of Exserohilum monoceras Inu-1, a fungal pathogen of Barnyard grass. The structure was determined by spectroscopic analyses including 2D NMR experiments. During the isolation procedure, the toxic components were monitored by the assay using Italian ryegrass (Lolium multiflorum Lam.), a host plant of the pathogen. The compounds inhibited the root growth of the host plant seedlings at a level of 100 ppm. While no substantial inhibition was observed even at 300 ppm in non-host plant seedlings such as lettuce and tomato.