Journal of the Chemical Society. Chemical communications p. 391 - 392 (1991)
Update date:2022-08-11
Topics:
Basile, Tiziana
Longobardo, Luigi
Tagliavini, Emilio
Trombini, Claudio
Umani-Ronchi, Achille
The stereoselectivity of the Lewis acid induced acylation of open-chain silyl enol ethers by chiral orthoesters is strongly affected by the C=C bond configuration: both Z and E silyl enol ethers are acylated in good isolated yields, but the Z isomers give
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