63473-85-8Relevant articles and documents
ORGANOMANGANESE(II) REAGENTS XXII. COPPER-CATALYZED CONJUGATE ADDITION OF ORGANOMANGANESE REAGENTS TO α,β-ETHYLENIC ESTERS.
Cahiez, Gerard,Alami, Mouad
, p. 7423 - 7424 (1990)
Copper-catalyzed conjugate addition of organomanganese reagents to α,β-ethylenic esters easily takes place in THF at 0 deg C, in the presence of 3 percent CuCl and Me3SiCl.Good to moderate yields are obtained from organomanganese reagents prepared from organolithium or organomagnesium compounds.
Efficient kinetic resolution in the asymmetric hydrosilylation of imines of 3-substituted indanones and 4-substituted tetralones
Yun, Jaesook,Buchwald, Stephen L.
, p. 767 - 774 (2007/10/03)
Kinetic resolution of the N-methyl imines of 3-substituted indanones and 4-substituted tetralones could be accomplished by hydrosilylation with a chiral titanocene catalyst. N-Methyl imines of 4-substituted tetralones were resolved to yield, after hydrolysis of the unreacted starting materials, ketones with high ee's and the amine products with high diastereomeric and enantiomeric purity. The utility of this process was demonstrated in the synthesis of sertraline.