A simple and practical synthetic method for the cinnamonitriles and cinnamic acids was pre- sented.

Under microwave irradiation,cinnamonitrile was prepared directly from cinnamaldehyde/NH_2OH·HCl in the presence of SiO_2/K_2CO_3 under solvent-free condition in one step.

The reaction of substituted cinnamonitriles with 5,5-dimethyl-1,3-cyclohexanedione in 95% ethanol catalyzed by KF-montmorillonite, provides a fast, efficient and high-yielding access to 2-amino-3-cyano-4-aryl-7,7-dimethyl-5-oxo-4H-5,6,7,8-tetrahydrobenzo[b]pyran.

The reactions of substituted cinnamonitriles with β-naphthol proceed very efficiently in water in the presence of triethylbenzylammonium chloride (TEBA) to give naphthopyran derivatives, which were isolated simply by filtration.

Synthesis and characterization of new perfume α-amylcinnamonitrile;

Study on the purifying technology of the total saponins in cinnamon by macroporous resin;

Determination of Cinnamaldehyde and Cinnamic Acid in Cinnamon by Non-aqueous Capillary Electrophoresis with UV Detection;

Study on Technique of Cinnamon Volatile Oil by Supercritical Fluid Extration;

Investigation on Germanium in Cinnamomum Cassia Presl by Spectrophotometry;

Methodological Study on GC Fingerprint of Volatile Oil from Cinnamomum cassia Presl;

Chemical Components of Essential Oils of Cinnamomum cassia Presl. in Different Growth Year;

Analysis on the Chemical Compositions of the Volatile Oil from Ultramicro-powder and Common Grinding Powder of Cinnamomum cassia;

Determination of cinnamic acid in Cinnamomum cassia presl after compatibility in Coptis chinensis Franch;