Stereochemical control of tertiary alcohol: aldol condensation of lactate derivatives

@article{Kamino2001StereochemicalCO,
  title={Stereochemical control of tertiary alcohol: aldol condensation of lactate derivatives},
  author={T. Kamino and Yoshihisa Murata and N. Kawai and S. Hosokawa and Susumu Kobayashi},
  journal={Tetrahedron Letters},
  year={2001},
  volume={42},
  pages={5249-5252}
}
Abstract Stereoselective construction of aldol adducts having tertiary alcohol at the α position was achieved via a titanium(IV) enolate derived from a lactate derivative with an Evans chiral auxiliary. The stereochemistry at α-tertiary alcohol could be controlled by selecting the protective group of the starting lactate. 
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