87241-25-6Relevant articles and documents
UNSYMMETRICAL MONOPROTECTED α-DIKETONES VIA THE PALLADIUM-CATALYZED VINYLATION OF ACID CHLORIDES WITH ORGANOTIN COMPOUNDS
Soderquist, John A.,Leong, William Wei-Hwa
, p. 2361 - 2362 (1983)
Under benzyl(chloro)bis triphenylphosphinepalladium(II) catalysis, α-oxygenated vinyltin compounds undergo clean cross coupling with acid chlorides to give α-oxygenated enones which are converted to unsymmetrical α-diketones, butadienyl ethers or substituted methyl vinyl ketones.