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Metabolism of 2,4',5-trichlorobiphenyl by the mercapturic acid pathway

โœ Scribed by Bakke, J.; Bergman, A.; Larsen, G.


Book ID
121489906
Publisher
American Association for the Advancement of Science
Year
1982
Tongue
English
Weight
681 KB
Volume
217
Category
Article
ISSN
0036-8075

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Synthesis of 2,4โ€ฒ,5-trichloro [14C]biphe
โœ Ake Bergman; Jerome E. Bakke; Vernon J. Feil ๐Ÿ“‚ Article ๐Ÿ“… 1983 ๐Ÿ› John Wiley and Sons ๐ŸŒ French โš– 286 KB

The synthesis of 3-and 4-S-(N-acetyl)cysteinyl-2,4' ,5-tri~hloro?~CJbiphenyl is described. 4-ChloroC Claniline was used as starting material. The products were obtained after an aryl coupling of the amine with 2,5-dichloronitrobenzene, a reduction of the nitrogroup and finally coupling of the diazot