Säurekatalysierte Umlagerungen von 1,5-Dimethyl-6-methyliden-tricyclo[3.2.1.02,7]oct-3-en-8endo-olen

Acid Catalysed Rearrangement of 1,5-Dimethyl-6-methyliden-tricyclo[3.2.1.0^2,7]oct-3-en-8endo-ols The tricyclic alcohols 2,3,4 and 6 (Scheme 1) are synthesized by the reaction of the tricyclic ketone 1 with sodiumborohydrid or metalloorganic reagents. Their configuration at C(8) is determined by NMR. in the presence of Eu(fod)₃. The exo-attack of 1 by the nucleophil forming the endo-alcohol is favored, the π-electrons of C(3) = C(4) hindering the endo-attack. On treatment with sulfuric acid in dioxane/water at 25° the tertiary alcohols yield aryl-substituted ketones. 3 gives in 78.5% yield a mixture of the 3-(dimethylphenyl)-2-butanones 12 and 13 , in addition to 16.5% of (2,3,4-trimethylphenyl)-2-propanon ( 14 ) (Scheme 2). The alcohols 4 and 6 yield mixtures of the 2-(dimethylphenyl)-3-pentanones 19 and 20 (72%), and 2-(dimethylphenyl)-propiophenones 21 and 22 (68%), respectively (Scheme 2). In the case of the secondary alcohol 2 mainly products derived from hydration at the C(6), C(9) double bond are formed, namely the mixture of diols 23 and 24 (21%), and the mixture of the isomeric 2-(dimethylphenyl)propanals 25, 26 and 27 (3%) (Scheme 3). - The structures of 12–14, 19/20, 21/22, 23/24 and 25/26/27 were established by spectroscopic data. In the case of 12 and 13 the degradation of their mixture to the known 1-(dimethylphenyl)ethanols 17/18 confirmed the assignment. - The most probable mechanism for the rearrangement of 3 is shown in Schemes 4 and 5. The reaction proceeds from 3 through a, b and g to 12 and 13; 14 is formed via e, f and i . In the case of 4 and 6 only the reaction analogue to 3 → a → b → g ?12/13 takes place. The isomeric aldehyds 25–27 formed from 2 could have the structures s, t , and v . The former two could be generated in a similar way as 12/13 from 3 , the latter one as shown in Scheme 8.     

Eptastigmine,nicotinamide and nicotinic acid determination using an inhibition enzyme sensor; application to pharmaceutical analysis

An enzyme inhibition biosensor, developed in our laboratory and previously used for the analysis of compounds with anticholinesterase activity (e.g. physostigmine, neostigmine, pyridostigmine nicotine and organophosphorus compounds) has now been tested for the analysis of another recently synthesized cholinesterase inhibitor, i.e. eptastigmine. In addition nicotinic acid and nicotinamide, although displaying weaker inhibition properties, were also tested in pharmaceutical products using the same inhibition enzyme sensor. The biosensor consisted of a hydrogen peroxide amperometric electrode coupled to a functionalised nylon membrane chemically bonding both the enzymes butyrylcholinesterase and choline oxidase; a butyrylcholine standard solution in glycine buffer acted as substrate. The response of the system to all the inhibitors considered was characterised completely and the analysis of several pharmaceutical formulations containing nicotinamide or nicotinic acid was also performed.     

Un teorema di Radon-Nikodym per funzioni d’insieme subadditive

Riassunto In questo articolo si danno delle condizioni necessarie e sufficienti affinchè per una fissata coppia di funzioni d’insieme ν, μ crescenti esista una funzionef tale che ν=∫fdμ. Si ottiene cosi una proposizione comprendente il teorema di R-N. classico e dei teoremi di R-N., presentati da altri autori, riguardanti le funzioni d’insieme finitamente additive e le funzioni d’insieme subadditive e continue per successioni crescenti.

---

Résumé Soient ν, μ:A→[0,+∞) deux fonctions d’ensemble croissantes sur une σ-algèbre d’ensemblesA⊂T(X), telles que pour chaqueA∈A avec ν(A)=μ(A)=0 on a l’égalité μ(A)=μ(A∪S) ∀S∈A (c’est le cas des fonctions sousadditives!). Dans cet article on démontre qu’il existe une fonctionf A-measurable telle que ν=∫fdμ si et seulement si pour chaquer∈(0, + ∞) il y a un ensembleA _r∈A qui vérifie les trois conditions suivantes: (1) ,B∈A avecB⊂A; (2) A (3) limν(A _r)=0. On déduit ainsi une proposition qui a été donnée parI. Forana: ?Si ν, μ sont simplement additives, il existe une fonctionf telle que ν=∫fdμ si et seulement si ν≪μ et la fonction d’ensemble additive a une decomposition de Hahn pour chaquer∈(0, + ∞), c’est-á-dire il y aA _r∈A tel que ?.

     

Unimodular lattices with long shadow

Let L be an odd unimodular lattice of dimension n with shadow n−16. If min(L)?3 then dim(L)?46 and there is a unique such lattice in dimension 46 and no lattices in dimensions 44 and 45. To prove this, a shadow theory for theta series with spherical coefficients is developed.     

A finite algorithm for solving general quadratic problems

Here we propose a global optimization method for general, i.e. indefinite quadratic problems, which consist of maximizing a non-concave quadratic function over a polyhedron inn-dimensional Euclidean space. This algorithm is shown to be finite and exact in non-degenerate situations. The key procedure uses copositivity arguments to ensure escaping from inefficient local solutions. A similar approach is used to generate an improving feasible point, if the starting point is not the global solution, irrespective of whether or not this is a local solution. Also, definiteness properties of the quadratic objective function are irrelevant for this procedure. To increase efficiency of these methods, we employ pseudoconvexity arguments. Pseudoconvexity is related to copositivity in a way which might be helpful to check this property efficiently even beyond the scope of the cases considered here.     

Middle ear prosthesis: significance in magnetic resonance imaging

The Armstrong model of the Schuknecht gel foam and wire prosthesis was tested in the magnetic field of a 1.5 Tesla magnet. The wire component of the prosthesis was found to be non-magnetic. Patients with this prosthesis can therefore undergo MRI examination safely. Two previous articles from the non radiologic literature concerning the magnetic properties of metallic middle ear prostheses are reviewed.     

Magnetism of an Fe65Mn35 alloy in the fcc/hcp phase region

Among the three possible phase structures (bcc, fcc and hep) of iron rich Fe₁₀₀-cMn _c alloys (c _Mn <40 at%), the two closed packed structures, fcc and hep, produce poor resolved and similar Mössbauer spectra. Therefore the evaluation of spectra collected on a sample (nominalc _Mn =35 at%) with coexisting fcc and hep phases only was possible with the help of the Afans’ev/Tsymbal method of “Mössbauer lines sharpening” introduced recently/1,2,3/. A comparison of the hyperfine field vs. temperature with an FeNi-Invar alloy (c _Ni =35 at%) shows a surprising similarity.