Préparation et oxydation anodique d'acides β-cétaliques. Application à la synthèse de γ-bisdioxolannes symétriques et des γ-dicétones dérivées

J Einhorn, JL Soulier, C Bacquet…

Index: Einhorn, Jacques; Soulier, Jean-Louis; Bacquet Cathy; Lelandais Daniel Canadian Journal of Chemistry, 1983 , vol. 61, p. 584 - 587

Full Text: HTML

Citation Number: 8

Abstract

Anodic oxidation of carboxylic acids with β-dioxolane substituents leads to good yields of symmetrical γ-bisdioxolanes. Hydrolysis of these compounds easily provides the corresponding γ-diketones. The synthesis of the starting acids is described.[Journal translation]

Related Articles:

Oxazaborolidine-catalysed reduction of alk-2-ene-1, 4-diones. A convenient access to chiral 1, 4-diols

[Bach, Jordi; Berenguer, Ramon; Garcia, Jordi; Lopez, Marta; Manzanal, Judith; Vilarrasa, Jaume Tetrahedron, 1998 , vol. 54, # 49 p. 14947 - 14962]

Oxazaborolidine-catalysed reduction of alk-2-ene-1, 4-diones. A convenient access to chiral 1, 4-diols

[Tetrahedron, , vol. 54, # 49 p. 14947 - 14962]

Influence of the stereochemistry on the 1, 2-dialkenylcyclobutanols behaviour: oxy-cope versus retro-ene rearrangements

[Tetrahedron Letters, , vol. 30, # 19 p. 2525 - 2528]

Reaction of ketone enolates with copper dichloride. Synthesis of 1, 4-diketones

[Journal of the American Chemical Society, , vol. 97, p. 2912 - 2914]

Préparation et oxydation anodique d'acides β-cétaliques. Application à la synthèse de γ-bisdioxolannes symétriques et des γ-dicétones dérivées

[Canadian Journal of Chemistry, , vol. 61, p. 584 - 587]

More Articles...