852292-29-6

Upstream product

• 6293-83-0 2-iodo-4-nitrophenylamine 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 852292-40-1 N-[2-(3-hydroxy-prop-1-ynyl)-4-nitro-phenyl]-4-methyl-benzenesulfonamide 
• 852292-64-9 2-[3-[5-Nitro-2-(toluene-4-sulfonylamino)-phenyl]-prop-2-yn-(E)-ylidene]-succinic acid 1-ethyl ester 
• 1314595-87-3 2-((((2R,3S,6S)-2-(methoxymethyl)-6-phenyl-3,6-dihydro-2H-pyran-3-yl)oxy)methyl)-5-nitro-1-tosyl-1H-indole 
• 1314596-01-4 (R)-2-methoxy-1-((3S,4S)-6-nitro-4-((E)-styryl)-9-tosyl-1,3,4,9-tetrahydropyrano[3,4-b]indol-3-yl)ethanol 
• 1314596-02-5 (R)-2-methoxy-1-((3S,4R)-6-nitro-4-((E)-styryl)-9-tosyl-1,3,4,9-tetrahydropyrano[3,4-b]indol-3-yl)ethanol 
• 1433218-69-9 N-(2-bromoethyl)-N-(2-iodo-4-nitrophenyl)-4-methylbenzenesulfonamide 
• 1433218-51-9 C₁₅H₁₄N₂O₄S₂ 
• 852292-52-5 4-methyl-N-[4-nitro-2-(3-oxo-prop-1-ynyl)-phenyl]-benzenesulfonamide 

Relevant academic research and scientific papers

Palladium-Catalyzed Regioselective Synthesis of 1-Hydroxycarbazoles Under Aerobic Conditions

A palladium-catalyzed aerobic C?H amidation of N-Ts-2-amino-3′-hydroxylbiaryls has been developed to afford a diverse range of 1-hydroxycarbazoles with high regioselectivity and efficiency. This protocol benefits from operational simplicity, robustness, a

Synthesis of 2-BMIDA 6,5-bicyclic heterocycles by Cu(i)/Pd(0)/Cu(II) cascade catalysis of 2-iodoaniline/phenols

A one-pot cascade reaction for the synthesis of 2-BMIDA 6,5-bicyclic heterocycles has been developed using Cu(i)/Pd(0)/Cu(ii) catalysis. 2-Iodoanilines and phenols undergo a Cu(i)/Pd(0)-catalyzed Sonogashira reaction with ethynyl BMIDA followed by in situ Cu(ii)-catalyzed 5-endo-dig cyclization to generate heterocyclic scaffolds with a BMIDA functional group in the 2-position. The method provides efficient access to borylated indoles, benzofurans, and aza-derivatives, which can be difficult to access through alternative methods.

Palladium-catalyzed intramolecular reductive cross-coupling of Csp 2-Csp3 bond formation

A Pd-catalyzed efficient reductive cross-coupling reaction without metallic reductant to construct a Csp2-Csp3 bond has been reported. A PdIV complex was proposed to be a key intermediate, which subsequently went through d

Efficient access to 1,4-benzothiazine: Palladium-catalyzed double C-S bond formation using Na2S2O3 as sulfurating reagent

A novel Pd-catalyzed double C-S bond formation coupling reaction has been developed. This protocol, in which Na2S2O3 was used as sulfurating reagent in metal-catalyzed reactions, provides an efficient method for the synthe

A new preparative route to substituted carbazoles by benzannulation

A new regioselective pathway to substituted carbazole derivatives is described here. According to this procedure substituted 2-alkoxycarbonyl-4- acetoxy-9-(p-toluenesulfonyl) carbazoles are obtained by treatment of substituted 6-[2-(p-toluenesulfonyl-amin