Preparation et reactivite du derive lithie issu du dioxolanne du-ceto pentanoate de trimethylsilyle.
JL Moreau, R Couffignal
Index: Moreau, Jean Louis; Couffignal, Rene Tetrahedron Letters, 1982 , vol. 23, # 50 p. 5271 - 5274
Full Text: HTML
Citation Number: 1
Abstract
Résumé The organolithium reagent 4 issued from trimethylsilyl 4, 4-ethylendioxypentanoate 3 reacts with ketones; it affords β-hydroxy-acids 7 and β-ethylenic ketones 8. This reaction is an efficient route for carbonyl olefination. 4 also acts towards mixed carboxylic and carbonic anhydrides as a homoenolate equivalent.
Related Articles:
[Mikolajczyk, Marian; Midura, Wanda; Grzejszczak, Slawomir Tetrahedron Letters, 1984 , vol. 25, # 23 p. 2489 - 2492]
[Ballini, Roberto; Bosica, Giovanna; Fiorini, Dennis; Petrini, Marino Tetrahedron Letters, 2002 , vol. 43, # 30 p. 5233 - 5235]
[Stetter, Hermann; Lorenz, Guenther Chemische Berichte, 1985 , vol. 118, # 3 p. 1115 - 1125]
[Stetter,H.; Kuhlmann,H. Chemische Berichte, 1976 , vol. 109, p. 3426 - 3431]
Transition metal-catalysed acylation of α, β-unsaturated carbonyl compounds with acylstannanes
[Shirakawa; Yamamoto; Nakao; Tsuchimoto; Hiyama Chemical Communications, 2001 , # 19 p. 1926 - 1927]