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Identification of heterocyclic compounds

Identification of the product(s) resulting from the reaction of heterocyclic compounds with diazomethane has been used in attempts to elucidate their tautomeric composition (for summaries, see references 7 and 41). This work was based on the assumption that if a compound which is capable of existing in both an —NH and an —OH form produced only the =NMe derivative when it w as treated with diazomethane, it existed entirely in the =NH form. On the other hand, formation of the —OMe derivative was interpreted to mean that a finite amount of the compound existed in the —OH form. In some cases the tautomer present in the solid state w as concluded to be different from that present in solution for example, 41 42 gave a higher proportion of the 3,4-dimethoxy derivative when ethereal diaz-... [Pg.324]

Tabakovic, I. Anodic Synthesis of Heterocyclic Compounds. 185, 87-140 (1997). Takahashi, Y. Identification of Structural Similarity of Organic Molecules. 174, 105-134... [Pg.183]

Stick RV (1997) The Synthesis of Novel Enzyme Inhibitors and Their Use in Defining the Active Sites of Glycan Hydrolases. 187 187-213 Stutz AE, see de Raadt A (1997) 187 157-186 Stumpe R, see Kim JI (1990) 157 129-180 Suami T (1990) Chemistry of Pseudo-sugars. 154 257-283 Suppan P (1992) The Marcus Inverted Region. 153 95-130 Suzuki N (1990) Radiometric Determination of Trace Elements. 157 35-56 Tabakovic I (1997) Anodic Synthesis of Heterocyclic Compounds. 185 87-140 Takahashi Y (1995) Identification of Structural Similarity of Organic Molecules. 174 105-134 Tasi G, Palinkd I (1995) Using Molecular Electrostatic Potentid Maps for Similarity Studies. 174 45-72... [Pg.320]

Diketones are used for extraction and identification of metals, and as raw materials for synthesis of heterocyclic compounds. The ability of... [Pg.499]

Abstract Considering the presence of multiple types of cell death induced by chemicals, it is important to determine a definitive strategy for the exploration of new highly tumor-selective compounds. The screening of highly selective compounds should be performed before the identification of the type of cell death (either apoptosis, autophagy, or necrosis) and the cell death induction mechanism. The tumor specificities of heterocyclic compounds and the type of cell death induced by them are summarized. [Pg.173]

Synthesis of large number of heterocyclic compounds corresponding to the chemical concept led to the identification of the im-idazopyridine class of compounds. [Pg.237]

P Dugo, L. Mondello, E. Sebastian , R. Ottana, G. Eirante and G. Dugo, Identification of minor oxygen heterocyclic compounds of citi us essential oils by liquid chromatography-atmospheric pressure chemical ionisation mass specti ometiy , J. Liq. Chromatogr. 22 2991-3005 (1999). [Pg.133]

For the purpose of polymer/additive analysis most applications refer to vulcanisate analysis. Weber [370] has determined various vulcanisation accelerators (Vulkazit Thiuram/Pextra N/Merkapto/AZ/DM) in rubbers using PC. Similarly, Zijp [371] has described application of PC for identification of various vulcanisation accelerator classes (guanidines, dithiocarbaminates, thiuramsulfides, mercapto-substituted heterocyclic compounds, thioureas, etc.). The same author has also... [Pg.220]


See other pages where Identification of heterocyclic compounds is mentioned: [Pg.29]    [Pg.29]    [Pg.146]    [Pg.29]    [Pg.29]    [Pg.29]    [Pg.29]    [Pg.146]    [Pg.29]    [Pg.29]    [Pg.1217]    [Pg.198]    [Pg.327]    [Pg.547]    [Pg.261]    [Pg.166]    [Pg.128]    [Pg.28]    [Pg.9]    [Pg.186]    [Pg.180]    [Pg.41]    [Pg.6]    [Pg.1]    [Pg.389]    [Pg.127]    [Pg.127]    [Pg.390]    [Pg.578]    [Pg.1004]    [Pg.9]    [Pg.926]   
See also in sourсe #XX -- [ Pg.106 , Pg.108 , Pg.109 , Pg.135 , Pg.137 ]




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Identification of compounds

Identification of heterocyclic

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