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  • 1980-1984  (3)
  • 1965-1969  (3)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of chemical information and modeling 21 (1981), S. 48-52 
    ISSN: 1520-5142
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 87 (1965), S. 3300-3303 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 8 (1967), S. 165-174 
    ISSN: 1432-2234
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Résumé La pratique habituelle, qui consiste à corréler la réaotivité et un indice particulier de la méthode des orbitales moléculaires, ne tient pas compte des variations relatives de réactivité des différentes positions d'un donneur d'électrons conjugué avec la nature du réactif électrophile. En considérant la formation de l'état de transition comme une perturbation mutuelle des orbitales moléculaires des deux réactifs, la réactivité relative des différents centres réactifs varie avec l'importance de la perturbation. Notre travail détermine les facteurs responsables de ces variations de réactivité. Il définit les conditions ou les orbitales frontiéres peuvent déterminer le cours d'une réaction, et attire l'attention sur l'importance de l'interaction électrostatique.
    Abstract: Zusammenfassung Im Rahmen der MO-Theorie wird die Reaktivität gewöhnlich nur zu gewissen Indizes in Verbindung gesetzt. Damit ist die Reaktivität an den verschiedenen Zentren eines konjugierten Donators aber unabhängig von der Art des elektrophilen Agens. Wenn man den Übergangszustand als eine wechselseitige Störung der Molekülorbitale beider Agentien auffaßt, ändert sich die relative Reaktivität verschiedener Zentren mit der Größe dieser Störung. Dieses Verfahren bestimmt verschiedene Faktoren, die für den Wechsel in der Reaktivität verantwortlich sind. Es erklärt, unter welchen Bedingungen die „Grenzorbitale“ den Verlauf einer Reaktion bestimmen und verweist auf die Bedeutung von elektrostatischen Wechselwirkungen.
    Notes: Abstract The usual practice of relating reactivity to a particular MO index does not allow for changes in the relative reactivity of various positions in a conjugated electron donor with the nature of the electrophilic reagent. By regarding the formation of the transition state as a mutual perturbation of the Molecular Orbitals of both reagents, the relative reactivity of various reacting centers is shown to vary with the magnitude of the perturbation. This treatment determines the factors responsible for these changes in reactivity. It outlines the conditions under which the frontier orbitals may determine the course of a reaction and also draws attention to the importance of electrostatic interaction.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Molecular mechanics calculations have been used to determine the preferred physical association sites of the known alkylating agent dimethyl aziridinium ion (Az+) and a CH3+ prototype test probe with B-form, tetrameric DNA sequences. Electrostatic interactions are most important in determining these preferential physical association sites. In turn, the intermolecular energy minima depend on the charge distribution assigned to the DNA sequence. However, for three reported DNA charge distributions, only two distinct sets of energy minima were obtained for the CH3+-like ion interacting with (G-C)4, (A-T)4, and [(G-C)·(A-T)]2 deoxyribonucleic acids. These minima correspond to physical association geometries in which the CH3+-like ion is near known alkylation sites. The results of the Az+ … [(G-C)·(A-T)]2 interaction are virtually identical to those found for the CH3+-like ion. Aqueous solvation energetics have little effect on the physical association of Az+ with [(G-C)·(A-T)]2.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 19 (1980), S. 325-340 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of molecular orbital calculations, using MINDO/3 and CNDO/2L methods, have been used to characterize the chemical reaction of protonated aziridine with DNA nucleophilic base sites. The N-7 atom of guanine is found to be the preferred alkylation site only when the O-6 atom of guanine is involved in base-pair hydrogen bonding. Otherwise O-6 is the predicted major site of alkylation. This indirectly suggests that protonated aziridine alkylation processes involve base-paired DNA structures, since N-7 guanine is the observed major site of alkylation. Alkylation of N-3 adenine is predicted to be more favorable than chemical attack of the N-7 adenine position. Both of these sites, however, are predicted to be less reactive than N-7 of guanine. These chemical reactivity studies resolve alkylation specifically not achieved in the DNA-alkylator physical association calculations reported in the preceding paper.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 77 (1965), S. 460-460 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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