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Volatile organic compounds (VOCs) are produced by plants responding to biotic and abiotic stresses. According to their biosynthetic sources, induced VOCs are divided into three major classes: terpenoids, phenylpropanoid/benzenoid, and fatty acid derivatives. These compounds with specific aroma characteristics importantly contribute to the aroma quality of oolong tea. Shaking and rocking is the crucial procedure for the aroma formation of oolong tea by exerting mechanical damage to fresh tea leaves. Abundant studies have been carried out to investigate the formation mechanisms of VOCs during oolong tea processing in recent years. This review systematically introduces the biosynthesis of VOCs in plants, and the volatile changes due to biotic and abiotic stresses are summarized and expatiated, using oolong tea as an example. [ABSTRACT FROM AUTHOR]

A series of thiosemicarbazone derivatives of benzo-15-crown-5 were synthesized efficiently at room temperature using hydrogenchloride acid (HCl) as catalyst. Their anion recognition properties of a, b and c were studied, the result show they exhibit highly selective binding and sensing of F-, MeCO2- and n-C3H7CO2- in CH3CN (F- > n-C3H7CO2- > MeCO2- > > Cl-, Br- and I-). Especially receptor c shows different UV-Vis spectrum of F- from MeCO2-and C3H7CO2-, in addition to the color of the solution change from colorless to yellow upon the addition of F-, these two points make it suitable to be used as colorimetric anion sensor to identify fluoride anion from other halide anions and carboxylate anions by naked-eye. The connection between receptor and anion is by hydrogen bonding interactions, the binding ratio is 1:1, which have been confirmed by UV-vis inspection spectra in CH3CN and 1HMR in DMSO-d6. [ABSTRACT FROM AUTHOR]

9a-(3-Azabicyclo[3,3,1]nonanyl)-2'-cyclopentyl-2'-hydroxy-2'-phenylacetate (1) was synthesized and its enantiomers were obtained by the optical resolution of racemates with the chiral host N- p -toluenesulfonylglutamic acid. Optical pure 1 was also effective diastereoselective synthesized using benzaldehye as steric hindrance agent from the chiral starting material, ( S ) or ( R )-mandelic acid. The structure of the title compound was first elucidated by X-ray analysis. [ABSTRACT FROM AUTHOR]