Oxidative esterification of alkenes via π- and σ-organopalladium complexes: new pathways for the reaction
摘要:
New mechanistic data on the oxidative esterification of alkenes were obtained in the study of the reaction of Pd(II) acetate with hex-1-ene, methylcyclohex-1-ene and racemic a-pinene in a chloroform solution. High yields of unsaturated esters with terminal alcohol group were found in the oxidation of hex-l-ene, while the exocyclic methyl groups in methyleyclohex-1-ene and a-pinene remain untouched. (C) 2001 Elsevier Science B.V. All rights reserved.
New mechanistic data on the oxidative esterification of alkenes were obtained in the study of the reaction of Pd(II) acetate with hex-1-ene, methylcyclohex-1-ene and racemic a-pinene in a chloroform solution. High yields of unsaturated esters with terminal alcohol group were found in the oxidation of hex-l-ene, while the exocyclic methyl groups in methyleyclohex-1-ene and a-pinene remain untouched. (C) 2001 Elsevier Science B.V. All rights reserved.