Trapping experiment with aniline for a biosynthetic intermediate of sulfur-containing cruciferous phytoalexins

Journal of Organic Chemistry

Volumn 61, Issue 25, 1996, Pages 9053-9054

  Monde, Kenji ^a,b   Tanaka, Akiko ^a   Takasugi, Mitsuo ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

^b TOHOKU UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

BRASSICANAL A; PHYTOALEXIN; UNCLASSIFIED DRUG;

ARTICLE; BIOSYNTHESIS; NUCLEAR MAGNETIC RESONANCE; PHYTOCHEMISTRY; REACTION ANALYSIS; ULTRAVIOLET IRRADIATION;

EID: 0030474632     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo961506w     Document Type: Article

References (16)

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12. Monde, K.; Takasugi, M.; Ohnishi, T. J. Am. Chem. Soc. 1994, 116, 6650-6657.
13. Large-scale experiments were performed by adding acetanilide instead of aniline, due to the ease in handling. In either case, the same compound was obtained.
14. These peaks were shown to be due to phenylthioureas derived from aniline and respective isothiocyanates from corresponding glucosinolates (Tanaka, A. Unpublished results).
15. Monde, K.; Takasugi, M.; Lewis, J. A.; Fenwick, G. R. Z. Naturforsch., C: Biosci. 1991, 46, 189-193.
16. Monde, K.; Tamura, K.; Takasugi, M.; Kobayashi, K.; Somei, M. Heterocydes 1994, 38, 263-267.