Heck arylation of acrolein acetals using the 9-bromoanthracene: A case of study - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Journal of Organometallic Chemistry Année : 2008

Heck arylation of acrolein acetals using the 9-bromoanthracene: A case of study

Résumé

The influence of several parameters on the selectivity of the palladium catalysed Heck coupling of 9-bromoanthracene with acrolein acetals was studied. While the ester is the quasi exclusive product when only a base (i.e. NaOAc, K2CO3, etc.) is added in the medium, the presence of halide abstracting agent such as thallium or silver salts decreases noticeably the selectivity towards the ester. On the other hand, the addition of n-Bu4NOAc yields to the formation of the aldehyde with up to 74% selectivity. The presence of water was found to play a significant role not only on the rate but also on the selectivity of the reaction. A comprehensive mechanism is proposed outlining the influence of each additive, particularly on the selectivity of the reaction. (c) 2008 Elsevier B. V. All rights reserved.

Domaines

Catalyse

Dates et versions

hal-00474621 , version 1 (20-04-2010)

Identifiants

Citer

K. Pan, S. Noel, C. Pinel, L. Djakovitch. Heck arylation of acrolein acetals using the 9-bromoanthracene: A case of study. Journal of Organometallic Chemistry, 2008, 693 (17), pp.2863-2868. ⟨10.1016/j.jorganchem.2008.05.042⟩. ⟨hal-00474621⟩
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