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28
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0342880717
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note
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3CN, for 35 min, linear gradient, and a flow rate of 1.0 mL/min.
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29
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0343315677
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note
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2O extracts. No other metabolites derived from camalexin were detected in acidic or butanol extracts. The structures of the products were determined from analyses of the spectroscopic data (NMR, MS, FTIR, UV) of the purified (prep TLC) metabolites, and confirmed by chemical synthesis.
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-
-
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30
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0342880715
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note
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++1) (100).
-
-
-
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32
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0342446192
-
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note
-
+ + 18) (100).
-
-
-
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33
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84952543103
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3 and conversion of the resulting aldehyde to the nitrile using hydroxylamine hydrochloride and selenium dioxide, according to Sosnovsky, G.; Krogh, J. A.; Umhoefer, S. G. Synthesis 1979, 722.
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Synthesis
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Sosnovsky, G.1
Krogh, J.A.2
Umhoefer, S.G.3
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34
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0343315674
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note
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+ + 1) (100).
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-
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35
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0026597089
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Ayer, W. A.; Craw, P. A.; Ma, Y.; Miao, S. Tetrahedron 1992, 48, 2919.
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Ayer, W.A.1
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36
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0029615458
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Fu, X; Schmitz, F. J.; Tanner, R. S. J. Nat. Prod. 1995, 55, 1950.
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Fu, X.1
Schmitz, F.J.2
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37
-
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0342880713
-
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note
-
-5 M) was added to PDA medium at ca. 50 °C, mixed quickly and poured onto Petri plates. An agar plug (5 mm diameter) cut from edges of 5-day-old solid cultures of R. solani was placed upside down on the center of each plate, the plates sealed with parafilm, and incubated under constant light at 24 ± 2 °C for four days. The diameter of the mycelial covered area was measured daily. Control plates containing only PDA medium or PDA medium and DMSO were prepared and incubated similarly. Each assay was repeated at least twice, in triplicate.
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