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Kurt Günther Reinhold Carle Ilona Fleischhauer Stefan Merget 《Fresenius' Journal of Analytical Chemistry》1993,345(12):787-790
Summary A semi-preparative low-pressure liquid-chromatographic procedure using tribenzoylcellulose has been developed for the separation and isolation of the four -bisabolol stereoisomers. Stereochemical assignments were made by HPLC-polarimeter coupling and by using the authentical isomers. This method can be applied to the quality control of chamomile preparations, as it allows the detection of adulterations resulting from admixtures of synthetic -bisabolol. In addition, the isolation of all four -bisabolol stereoisomers from commercially available synthetic -bisabolol has been made possible. 相似文献
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C(alpha)-Formylglycine, the catalytic amino acid residue in the active site of sulfatases, is generated by post-translational modification of a cysteine or serine residue. We describe a highly sensitive procedure for the detection of C(alpha)-formylglycine-containing peptides in tryptic digests of sulfatase proteins. The protocol is based on the formation of hydrazone derivatives of C(alpha)-formylglycine-containing peptides when using dinitrophenylhydrazine as a matrix for matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOFMS). The hydrazone derivatives desorb and ionize with high efficiency and can be detected in the sub-femtomole range. The presence of C(alpha)-formylglycine is indicated by a mass increment of 180.13 u, corresponding to the hydrazone moiety, and also by a unique C-terminal fragment ion, characteristic of sulfatases, that becomes prominent in MALDI post-source decay mass spectra of the hydrazone derivatives. 相似文献
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- -VOPO4 (VO)2P2O7 . .
The specific activity and selectivity of (VO)2P2O7 in the oxidation of n-butane into maleic anhydride were found to be higher than those of -VOPO4. The important role of the (VO)2P2O7 crystal structure in mild oxidation of hydrocarbons is discussed.相似文献
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The literature data on heteropolar and homopolar 2-center bond dissociation energies in organic molecules in the gas phase and the corresponding heats of formation of radicals and ions have been critically evaluated. Data for more than 500 bonds are represented in tabular form together with the pertinent literature references. Selected electron affinities and π-bond dissociation energies have also been incorporated. The follow-up paper will discuss some empirical general aspects of these data particularly regarding the effect of structure on the bond dissociation energies. 相似文献
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MO calculations predict a P-C rotation barrier in triformylphosphine of less than 6 kcal/mol, and an inversion barrier of ca 14 kcal/mol. 相似文献