Journal of Organometallic Chemistry p. 1 - 12 (1985)
Update date:2022-09-26
Topics:
Moreau, Jean-Louis
Couffignal, Rene
At -60 deg C and in ether, the organolithium reagent produced by trimethylsilyl 4,4-ethylenedioxypentanoate reacts with aldehydes and ketones, and gives the expected β-hydroxyacids.The β-ethylenic ketones are isolated when the condensation is carried out
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Doi:10.1007/BF02158110
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