1679-09-0Relevant articles and documents
Reaction of Organocuprates with Dithio Esters: Double-Barrelled Carbophilic Addition and a New Synthetic Route to Tertiary Thiols
Bertz, Steven H.,Dabbagh, Gary,Williams, Lady M.
, p. 4414 - 4415 (1985)
Organocuprates prepared from lithium reagents or Grignard reagents react with dithio esters to give high yields of tertiary thiols; in the absence of Cu(I), only thiophilic addition products are observed.
Antimicrobial composition and method containing N-(3,5-dihalophenyl)-imide compounds
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, (2008/06/13)
Novel N-(3,5-dihalophenyl)imide compounds, which exhibit a strong antimicrobial activity against microorganisms including phytopathogenic fungi, parasites of industrial products and pathogenic microorganisms, represented by the formula, STR1 wherein X and X' each represent halogens and A represents a substituted ethylene such as chloroethylene, C1 - C4 alkylthioethylene, C1 - C2 alkyl-ethylene or 1,2-di-C1 - C2 -alkyl-ethylene, a cyclopropylene such as 1,3-dimethylcyclopropylene, trimethylene, a cyclohexylene-1,2-, cyclohexenylene-1,2-, cyclohexadienylene-1,2- or o-phenylene. The N-(3,5-dihalophenyl)imide compounds can be obtained by any of methods which produce imide compounds or reaction of an N-(3,5-dihalophenyl)maleimide compound with a mercaptan, a hydrogen halide, phosphorus chloride or thionylchloride.
