Journal
ADVANCED SYNTHESIS & CATALYSIS
Volume 349, Issue 3, Pages 281-286Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.200600467
Keywords
allylic substitution; asymmetric catalysis; Baylis-Hillman reaction; Cinchona alkaloids; hydrogen bond
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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.
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