L-функции Дирихле by Архангельская В. М.

By Архангельская В. М.

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This explains why numerous and extensive investigations have 38 V. Labet et al. been devoted to the characterization, measurement, and biological assessment (repair, mutagenic potential) of DNA lesions. More recently, major efforts have been made to complement the above information by using theoretical approaches for gaining further insights into the chemical reactivity of the bases. In the present chapter, emphasis is placed on the critical review of information gained from the use of density functional theory-based descriptors that shed new light on the endogenous and exogenous formation of several single and tandem lesions.

Experiment. Mol Phys 107:1187–1192 71. Reed AE, Weinstock RB, Weinhold F (1985) Natural population analysis. J Chem Phys 83:735–746 72. Bultinck P, Ayers PW, Fias S et al (2007) Uniqueness and basis set dependence of iterative Hirshfeld charges. Chem Phys Lett 444:205–208 73. Parr RG, Yang W (1984) Density functional approach to the frontier-electron theory of chemical reactivity. J Am Chem Soc 106:4049–4050 74. Ayers PW, Levy M (2000) Perspective on “density functional approach to the frontierelectron theory of chemical reactivity”.

Fraser HL, Floyd MB, Hopper DW (2007) Six-membered ring systems: pyridines and benzo derivates. In: Gribble GW, Joule JA (eds) Progress in heterocyclic chemistry, vol 18. Elsevier, Oxford 81. Ka¨llstro¨m S, Leino R (2008) Synthesis of pharmaceutically active compounds containing a disubstituted piperidine framework. Bioorg Med Chem 16:601–635 82. Felpin FX, Lebreton J (2003) Recent advances in the total synthesis of piperidine and pyrrolidine natural alkaloids with ring-closing metathesis as a key step.

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