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Downstream Products

• 1217811-13-6 N-(3,5-ifluorophenyl)-7-(diphenylmethylidene)bicyclo[2.2.1]hept-2-ene-5,6-dicarboximide 
• 1217743-47-9 N-(3,5-difluorophenyl)-7-[bis(4-bromophenyl)methylidene]bicyclo[2.2.1]hept-2-ene-5,6-dicarboximide 
• 1258432-62-0 N-(3,5-difluorophenyl)methylidene succinimide 
• 1258432-94-8 benzylidene-N-(3,5-difluorophenyl) succinimide 

Relevant academic research and scientific papers

Bicyclic guanidine-catalyzed direct asymmetric allylic addition of N-aryl alkylidene-succinimides

Enantio-enriched maleimides and succinimides that can be used to prepare aza-heterocycles with multiple chiral centers are obtained from the bicyclic guanidine-catalyzed direct asymmetric allylic addition of N-aryl alkylidene-succinimides to imines. NMR studies and deuterium-exchange experiments were used to study the intermediates in the reaction.

Antimicrobial composition and method containing N-(3,5-dihalophenyl)-imide compounds

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.