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Palladium-Catalyzed Formylation of Enol Triflates and lodoalkenes

Palladium-Catalyzed Formylation of Enol Triflates and lodoalkenes [Pg.234]

Formate salts [69] or formic add under conditions converting them electrodiemically into formate [70,71], sUyl, and tin hydrides have been also explored to perform formylations of organic halides/triflates under lower pressure of carbon monoxide. Acetic formic anhydride has been used as a source of carbon monoxide for the conversion of aryl iodides in conjunction with RsSiH [72]. The palladium-catalyzed formylation of a wide variety of vinyl iodides and triflates with tin hydride and carbon [Pg.234]

Trapping of 0(,P-Unsaturated Acylpalladium with Active C-H Compounds [Pg.235]

Acylpalladium complexes can be generated through an intramolecular carbopaUada-tion/carbonylation sequence of vinyl iodides/triflates bearing a proximate alkene or [Pg.235]




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Enol triflate

Enol triflates

Enolates palladium-catalyzed

Enolates triflate

Lodoalkenes

Palladium enolate

Palladium enolates

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