Abstract
Racemic Baylis-Hillman carbonates can be converted in densely functionalized products by reaction with cyano esters in the presence of a catalytic amount of a modified Cinchona alkaloid in high enantioselectivities and fair diastereoselectivities. A rational for the observed stereoselectivity is presented
Original language | Undefined/Unknown |
---|---|
Pages (from-to) | 281-286 |
Number of pages | 6 |
Journal | Advanced synthesis & catalysis |
Volume | 349 |
Issue number | 3 |
Publication status | Published - 2007 |