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Synfacts 2011(6): 0660-0660
DOI: 10.1055/s-0030-1259903
DOI: 10.1055/s-0030-1259903
Metal-Mediated Synthesis
© Georg Thieme Verlag
Stuttgart ˙ New York
A Stereoselective Approach to Tetrasubstituted Silyl Enol Ethers
Z. Song*, L. Kui, X. Sun, L. Li
Sichuan University, Chengdu and Lanzhou University, P. R. of China
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
19. Mai 2011 (online)

Significance
This work discloses a highly stereoselective approach to tetrasubstituted (Z)-β-hydroxy-α-TMS silyl enol ethers. The reaction proceeds via the addition of TMS-substituted oxiranyl anions to various aliphatic, aromatic, and heterocyclic acylsilanes. A subsequent Brook rearrangement leads to an intermediary siloxy carbanion, which after an epoxide opening affords tetrasubstituted, exclusively Z-configured silyl enol ethers.