97060-59-8Relevant articles and documents
Cerium(III) amide enolate. Addition of propionamide to conjugated enones
Shang,Liu
, p. 2155 - 2159 (2007/10/02)
The cerium(III) enolate of propionamide 1 was found to undergo preferential 1,2-addition with most of the sterically hindered conjugated enones studied. The effects of HMPA and 12-crown-4 on the regioselectivity were also investigated.
Stereoselection in the Michael Addition Reaction. 2. Stereochemistry of the Kinetic Michael Reaction of Amide Enolates with Enones
Heathcock, Clayton H.,Henderson, Mark A.,Oare, David A.,Sanner, Mark A.
, p. 3019 - 3022 (2007/10/02)
An extensive study of structure-stereoselectivity relationships in the kinetic Michael addition of preformed lithium enolates to enones has uncovered some reactions of sufficiently high diastereoselectivity as to be synthetically attractive and has allowe