38164-55-5

Upstream product

• 421-83-0 trifluoromethane sulfonyl chloride 
• 95-55-6 2-amino-phenol 
• 88-75-5 2-hydroxynitrobenzene 
• 132993-22-7 2-nitrophenyl trifluoromethanesulfonate 

Downstream Products

• 1334682-55-1 trifluoromethanesulfonic acid 2-(2,2-diethyl-3-oxo-butyrylamido)phenyl ester 
• 1334682-58-4 trifluoromethanesulfonic acid 2-(2-acetyl-2-isobutyl-4-methylpentanamido)phenyl ester 
• 1334682-53-9 (R,E)-3-hydroxy-3-styrylindolin-2-one 
• 1589523-10-3 (E)-3-(3-chlorostyryl)-2H-benzo[b][1,4]oxazin-2-one 
• 1589523-11-4 (E)-3-(4-chlorostyryl)-2H-benzo[b][1,4]oxazin-2-one 
• 1589523-09-0 (E)-3-styryl-2H-benzo[b][1,4]oxazin-2-one 
• 1589523-34-1 C₁₈H₁₆F₃NO₅S 
• 868234-57-5 (E)-3-(4-methoxystyryl)-2H-benzo[b][1,4]oxazin-2-one 
• 1334682-29-9 trifluoromethanesulfonic acid 2-(4-methyl-2-oxo-pentanoylamino)phenyl ester 
• 1334682-26-6 trifluoromethanesulfonic acid 2-(2-oxo-propionylamido)phenyl ester 
• 1396629-50-7 3-((4-methoxyphenyl)amino)-3-methylindolin-2-one 
• 1396629-44-9 3-methyl-3-((4-(trifluoromethyl)phenyl)amino)indolin-2-one 
• 1396629-25-6 3-isobutyl-3-(phenylamino)indolin-2-one 
• 1396629-21-2 3-methyl-3-(phenylamino)indolin-2-one 

Relevant academic research and scientific papers

Synthesis of enantiomerically enriched 3-amino-2-oxindoles through a palladium-mediated asymmetric intramolecular arylation of α-ketimino amides

A highly efficient and enantioselective synthesis of 3-amino-2-oxindoles through a palladium-catalyzed asymmetric intramolecular arylation of R-ketimino amides using (R)-DiFluorPhos as the coordinating ligand is reported. This report constitutes the first

Synthesis of enantiomerically enriched 3-amino-2-oxindoles through a palladium-mediated asymmetric intramolecular arylation of α-ketimino amides

A highly efficient and enantioselective synthesis of 3-amino-2-oxindoles through a palladium-catalyzed asymmetric intramolecular arylation of R-ketimino amides using (R)-DiFluorPhos as the coordinating ligand is reported. This report constitutes the first

A facile pathway to enantiomerically enriched 3-hydroxy-2-oxindoles: Asymmetric intramolecular arylation of α-keto amides catalyzed by a palladium-DifluorPhos complex

Less metal wastes: The first catalytic, enantioselective intramolecular aryl-transfer reaction of aryl triflates to ketones has been developed (see scheme; R1=R2=aromatic and aliphatic). This method features overall practicality, inc

Potassium organotrifluoroborates: New partners in palladium-catalysed cross-coupling reactions

The preparation of various potassium organotrifluoroborates bearing either aryl, alkenyl, or alkynyl substituents is described. These stable salts are shown to be very efficient partners in palladium-catalysed cross- coupling reactions with arenediazonium salts, affording biaryl and styrene derivatives in high yields.

Palladium-catalyzed cross-coupling reactions of arenediazonium tetrafluoroborates with aryl- And alkeriylboronic acids

Arcnediazonium tetrafluoroborates undergo a facile and efficient palladium-catalyzed cross-coupling reaction with aryl- and alkenylboronic acids at ambient temperature, without addition of base. The reaction described is characterized by a high chemoselectivity because bromide and trifiate functional groups are tolerated. Eisevier,.