1965
DOI: 10.1039/c19650000027
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Diacetoxyscirpenol and some related compounds

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1965
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Cited by 12 publications
(4 citation statements)
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“…The two compounds could inhibit egg hatch and immobilize second-stage juveniles of nematode M. incognita [73]. The two trichothecene compounds have been found in several other Fusarium species [74][75][76][77]. A new macrocyclic lactone derivative paeciloxazine (89) with the pyrrolobenzoxazine skeleton was isolated from the culture broth of Paecilomyces sp.…”
Section: Terpenoidsmentioning
confidence: 99%
“…The two compounds could inhibit egg hatch and immobilize second-stage juveniles of nematode M. incognita [73]. The two trichothecene compounds have been found in several other Fusarium species [74][75][76][77]. A new macrocyclic lactone derivative paeciloxazine (89) with the pyrrolobenzoxazine skeleton was isolated from the culture broth of Paecilomyces sp.…”
Section: Terpenoidsmentioning
confidence: 99%
“…Isolates of F. tricinctum produce a very potent toxin that has been charac- terized as 3-hydroxy-4, 15-diacetoxy-8-(3methylbutyryloxy) 12, 13-epoxy-A 9 trichothecene and has been designated as T-2 toxin (Bamburger et al, 1968). Another major toxic metabolite of F. tricinctum and F. roseum is diacetoxyscirpenol (3-hydroxy-4,15 diacetoxy-12,13-epoxy-A 9 -trichothecene) (Dawkins et al, 1965). These mycotoxins are colorless crystals with low water solubility.…”
Section: Introductionmentioning
confidence: 99%
“…Ein Signal bei 1,77 ppm ist der 16-Methylgruppe und ein breites Signal bei 5,3 ppm dem Vinylproton an C-8 zuzuordnen. Die Wasserstoffe an C-2, C-3 und C-11 verursachen Dublette bei 6= 4,27,5,56,3,99 rnit J = 3,5,3,5 und 4,O. Die Rruckeiibildung von C-10 nach C-13, die in analoger Weise aucli am [I] beobachtet worden ist, liess sich ebenso an Triacetoxyscirpenol…”
unclassified