Aza-Baylis-Hillman reaction is one important reaction,and have a lot of applications in organic chemistry.

A C—C bond forming reaction, namely Baylis-Hillman reaction, is described and the recent progress is reviewed in the study of the reaction mechanisms of the single molecular aldehyde and the double molecular aldehyde, TiCl4 catalytic mechanism, asymmetric induction mechanism, temperature and solvent effects as well as the ionic liquid reaction mechanism.

Baylis-Hillman reaction, which has great practical prospect, can be catalyzed by amine or phosphine.

The Baylis-Hillman reaction, a carbon-carbon bond forming reaction, is one of the very few re-actions wherein atom economy is perfectly preserved.

Synthesis and application of Chiral Organocatalysts in the Asymmetric Baylis-Hillman Reaction Chiral catalysts 1-4 were prepared conveniently from amino acids, and applied in asymmetric Baylis-Hillman reaction to study the relationship between catalyst structure and enantioselectivity.

Study on the Asymmetric Catalysis Morita-Baylis-Hillman Reactions;