113337-51-2Relevant articles and documents
Stereoselective synthesis of methyl (Z)-α-methoxyacrylates via two-carbon homologation of aldehydes
Baati, Rachid,Mioskowski, Charles,Kashinath, Dhurke,Kodepelly, Sanjeevarao,Lu, Biao,Falck
scheme or table, p. 402 - 405 (2009/05/11)
Methyl (Z)-α-methoxyacrylates are generated in good yields by a mild, stereospecific two-carbon homologation of a wide variety of aldehydes utilizing commercial methyl 2,2-dichloro-2-methoxyacetate and CrCl2 under Barbier conditions at room tem
A NOVEL APPROACH TO α-KETO ACID DERIVATIVES VIA PALLADIUM-CATALYZED ARYLATION AND VINYLATION OF METHYL α-METHOXYACRYLATE
Cacchi, Sandro,Ciattini, Pier Giuseppe,Morera, Enrico,Ortar, Giorgio
, p. 3039 - 3042 (2007/10/02)
Methyl α-methoxyacrylate reacts stereoselectively with aryl iodides and vinyl triflates under palladium catalysis to give enol ethers of arylpyruvates and of β,γ-unsaturated α-keto esters in good to moderate yields.