2.23
[]. Alfonso Pérez-Garrido, et al. Convenient QSAR model for predicting the complexation of structurally diverse compounds with beta-cyclodextrins. Bioorg Med Chem. 29 Jan 5;7(2):896-94.
[2]. Augusto Rivera, et al. FT-IR and DFT studies of the proton affinity of small aminal cages. Spectrochim Acta A Mol Biomol Spectrosc. 29 Oct ;74(2):588-9.
[3]. Cynthia D Selassie, et al. Cellular apoptosis and cytotoxicity of phenolic compounds: a quantitative structure-activity relationship study. J Med Chem. 25 Nov 7;48(23):7234-42.
[4]. G A Eiceman, et al. Atmospheric pressure chemical ionization of fluorinated phenols in atmospheric pressure chemical ionization mass spectrometry, tandem mass spectrometry, and ion mobility spectrometry. J Am Soc Mass Spectrom. 999 Nov;():57-65.
[5]. M F Carvalho, et al. Isolation and properties of a pure bacterial strain capable of fluorobenzene degradation as sole carbon and energy source. Environ Microbiol. 25 Feb;7(2):294-8.
H32-H35-H39-H335
P26-P264-P27-P27-P28-P32+P352-P34+P34-P33-P362+P364-P45-P5
GHS7