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  • A new approach to switching of enantioselectivity in NHC-Cu-catalyzed conjugate addition of alkylzincs to cyclic enones.

A new approach to switching of enantioselectivity in NHC-Cu-catalyzed conjugate addition of alkylzincs to cyclic enones.

Chemical communications (Cambridge, England) (2009-12-22)
Masaki Okamoto, Yuko Yamamoto, Satoshi Sakaguchi
ABSTRACT

Conjugate addition of Et(2)Zn to 2-cyclohexen-1-one catalyzed by Cu(OTf)(2) combined with an azolium salt derived from (S)-leucinol produced the corresponding (S)-adduct, while the use of Cu(acac)(2) in combination with the same ligand afforded the (R)-adduct as a major product.

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Sigma-Aldrich
2-Cyclohexen-1-one, ≥95%