101359-08-4

Upstream product

• 507233-69-4 triphenyl bismuth ⁽²⁺⁾; dichloride 
• 70-55-3 toluene-4-sulfonamide 
• 127-65-1 chloroamine-T 
• 603-33-8 triphenylbismuthane 
• 41123-35-7 triphenylbismuth diazide 
• 41083-16-3 triphenylbismuth dicyanide 

Downstream Products

• 75159-10-3 N-(4-methylbenzylidene)-p-toluenesulfonamide 
• 3157-65-1 N-(p-chlorobenzylidene)-p-toluenesulfonamide 
• 51608-60-7 N-(benzylidene)-p-methylbenzenesulfonamide 
• 6971-74-0 N-benzoyl-p-toluenesulfonamide 
• 3049-07-8 pentaphenylbismuth 
• 28899-97-0 triphenylbismuth(V) diacetate 
• 42967-53-3 tetraphenylbismuthonium chloride 
• 58593-03-6 {(C₆H₅)4Bi}⁽¹⁺⁾*(C₆H₅)3SiO^(1-)={(C₆H₅)4Bi}OSi(C₆H₅)3 
• 28719-55-3 triphenylbismuth dibromide 
• 6782-04-3 tetraphenylbismuthonium tetraphenylborate 
• 603-33-8 triphenylbismuthane 
• 13909-63-2 N-phenyl-N'-p-tolylsulfonylurea 
• 102-07-8 bis(diphenyl)urea 

Relevant academic research and scientific papers

Stabilized bismuthonium ylides bearing a highly cross-conjugated ylidic carbon atom: Synthesis, structures, and reactions

The reaction of iminotriaryl-λ5-bismuthanes (2; Ar3Bi=NR; R = COR″ or SO2R″) with dialkyl acetylenedicarboxylates (3; R′O2CC≡CCO2R′) has been found to afford highly stabilized bismuthonium ylides (4;

N-Tosyltriarylbismuthimines. Synthesis and Reactions with some Electrophiles

N-Tosyltriarylbismuthimines were prepared by the reaction of triarylbismuthines with chloramine-T and their properties were characterized.These bismuthimines reacted with aromatic aldehydes, acid chlorides, and isocyanates to form N-arylidene-tosylamides, N-aroyltosylamides, and N-aryl-N'-tosylureas, respectively.In the presence of copper catalyst, they readily decomposed into N-aryl- and N,N-diaryltosylamides, tosylamide, and triarylbismuthine.