Biochemisches Verhalten von Desoxyribonucleinsäure

Zusammenfassung Es wird eine durch DNS ausgel?ste biologische Wirkkette diskutiert. Durch DNS-Injektion lassen sich beim Warmblüter DNase-Aktivit?tserscheinungen hervorrufen. DNasen bewirken in niedrigen Konzentrationsbereichen 10⁻¹³-10⁻⁵ g/ml eine Steigerung der Zellzahl. In h?heren Konzentrationen wirken sie hemmend auf die Lebenst?tigkeit. Aufgrund dieser experimentellen Befunde ergibt sich ein selbstregelnder Mechanismus. Ausgeführt mit Mitteln der Deutschen Forschungsgemeinschaft.     

Eine quantitative Korrektur des durch gefärbte Lösungen hervorgerufenen Quench-Effektes bei der Flüssigscintillationsmessung

Analytical and Bioanalytical Chemistry -     

Biferrocenes and terferrocenes

Russian Chemical Bulletin -     

VI. Synthesis of Heterocyclic Analogs of γ-Aminobutyric Acid from 3,5-Dinitrobenzoic Acid

A series of 7-carboxy-3-R-1,5-dinitro-3-azabicyclo[3.3.1]non-6-enes was synthesized by reduction of 3,5-dinitrobenzoic acid with sodium borohydride followed by Mannich reaction with formaldehyde and primary amines. The mechanism of decomposition under electron impact of the 3-azabicyclo[3.3.1]nonane was established. Enthalpies of formation of compounds synthesized were calculated by semiempirical PM3 method.     

Hydrogention and Oxidation of Allyl Alcohol in the Presence of Colloid Palladium In Situ

Kinetic regularities of hydrogenation, oxidation with oxygen, and condensation of allyl alcohol in the presence of colloid palladium in situ were revealed. A mechanism of the reactions was proposed.     

Reaction of 2-chloro-5-methylbenzoquinone with Β-aminocrotonic ester derivatives

The reaction of 2-chloro-5-methylbenzoquinone with -aminocrotonic ester derivatives was studied by PMR spectroscopy in CD₃COOD. The spectra indicate the formation of intermediate hydroquinone and quinone derivatives, which subsequently transform into the corresponding indoles. It was shown that the indolization proceeds unequivocally at the 3-position of the initial benzoquinone, and the rate of formation of the indole derivatives decreases with increase in the size of the substituent at the nitrogen atom of the -aminocrotonic ester. The starting, intermediate compounds and the end products observed in the PMR spectra were identified by comparison with specially synthesized compounds.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 324–328, March, 1990.