958264-19-2

Upstream product

• 33925-51-8 2,2-diphenyl-4-methyl-4-pentenenitrile 
• 1037211-09-8 N-benzyloxycarbonyl-N'-(4-[dimethylazaniumylidene]-1,4-dihydropyridin-1-ylsulfonyl)azanide 
• 53001-08-4 4-methyl-2,2-diphenyl-pent-4-enylamine 

Downstream Products

• 958264-34-1 C₂₆H₂₆N₂O₄S 
• 1648743-89-8 (R)-benzyl 3a-methyl-5,5-diphenyltetrahydropyrrolo[1,2-b][1,2,5]thiadiazole-2(3H)-carboxylate-1,1-dioxide 
• 1648743-90-1 (S)-benzyl 3a-methyl-5,5-diphenyltetrahydropyrrolo[1,2-b][1,2,5]thiadiazole-2(3H)-carboxylate-1,1-dioxide 
• 1648744-02-8 (R)-(2-methyl-4,4-diphenylpyrrolidin-2-yl)methanamine 

Relevant academic research and scientific papers

Enantioselective diamination with novel chiral hypervalent iodine catalysts

Vicinal diamines constitute one the most important functional motif in organic chemistry because of its wide occurrence in a variety of biological and pharmaceutical molecules. We report an efficient metal-free, highly stereoselective intramolecular diamination using a novel chiral hypervalent iodine reagent together with its application as an efficient catalyst for the synthesis of diamines.

Exploring the nickel-catalyzed oxidation of alkenes: A diamination by sulfamide transfer

(Chemical Equation Presented) Nickel can oxidize, too! Nickel (II) salts such as nickel chloride and nickel acetylacetonate catalyze the intramolecular diamination of alkenes with urea and guanidine derivatives as well as sulfamides as nitrogen sources. T