Magydardiendiol,diterpenoid with a new skeleton from magydaris panacifolia (umbelliferae).

Three new diterpenoids with a substituted α-cyclogeraniol skeleton have been isolated from the umbelliferae $\text{Magydaris panacifolia}$ (Vahl) Lange, for which the names of magydar-2,13-dien-11,17-diol, $\text{1}$, magydar-2,10 (20), 13-trien-17-ol, $\text{2}$, and magydar-2,10(20), 13-trien-17-yl acetate, $\text{3}$, are proposed. The structures of these substances have been deduced from spectroscopic and chemical data.     

Chimie des complexes de metaux de transition avec des hydrocarbures cyanes : III. Quelques observations sur la conformation et la reactivite de complexes dicyclopentadienyles du molybdene et du tungstene

A new class of cyclic telluronium salts has been prepared. All the salts are stable in solution in CHCl₃ or dimethylsulphoxide (DMSO). Conductivity measurements in DMSO and dimethylformamide (DMF) have shown that considerable ion pairing occurs in solution. Infrared, ¹H, ¹³C, ¹²⁵Te NMR, and mass spectra are reported and discussed.     

CHEMILUMINESCENCE FROM THE OXIDATION OF AUXIN DERIVATIVES

Abstract— The thiophenyl ester of indole-3-acetic acid and indole-3-acetonitrile produce chemiluminescence in aerated dimethylsulfoxide in the presence of potassium t -butoxide. The emitter is the aromatic aldehyde. In the case of acetonitrile, the other product expected from the cleavage of an intermediate dioxetane, cyanate/isocyanate, has also been identified. Other auxins also chemiluminesce under similar conditions, but the emitters have not been properly identified.
These systems are models for the peroxidase catalyzed oxidation of indole-3-acetic acid to indole-3-carboxaldehyde and as such support the earlier inference (Vidigal et al , 1975) that the excited aldehyde is generated in the enzymic process.
An additional result is the observation of an exciplex between excited indole-3-carboxaldehyde and the thiophenylester of indole-3-acetic acid. This appears to be the first case of chemical generation of an exciplex by a route other than radical ion reaction, presumably by the dioxetane route.     

Energy dependence of the epithermal neutron spectrum shape parameter α with respect to application of comparator-type NAA

The epithermal neutron spectrum shape parameter in nuclear reactors is explained from a theoretical point of view in terms of the neutron slowing down density function. The latter is approximated by Fermi's age theory. Values for are calculated for a simple approximation of a nuclear reactor: a disk shaped fission neutron source in an infinite graphite moderator. The model produces -values with the correct sign and magnitude, compared to experimental values from the literature, determined in a real reactor. It is shown that varies strongly with distance to the neutron source and less strongly with neutron energy. The inappropriateness of average -values, obtained from the slope of quasi-straight lines produced by log-log plots of E^– versus E, for the correction of non-ideal epithermal neutron activation is discussed. Conclusions are formulated concerning the impact of an energy dependent on comparator type NAA.     

Laser photolysis study of the triplet states of nitroaromatic amides

The spectrokinetic indices of the triplet states of nitroaromatic amides were established. The quenching of triplet states by tertiary aromatic amines in apolar solvents leads to the formation of triplet exciplexes. A charge transfer state makes the major contribution to the structure of these exciplexes. Hydrogen atom transfer proceeds efficiently in the case of secondary aromatic amines, leading to the formation of the corresponding neutral radicals.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 8, pp. 1912–1915, August, 1989.     

Rapid and sensitive liquid chromatographic determination of carbamazepine suitable for use in monitoring multiple-drug anticonvulsant therapy.

A rapid, sensitive and selective method for the determination of carbamazepine and its major metabolite in plasma has been developed. Other commonly used anticonvulsants can be determined in the same procedure without interference. After extraction with dichloromethane, the components are separated by high-pressure liquid chromatography without further clean-up or concentration on a column packed with small-particle silica gel. The mean recovery from plasma is 98.6% with a relative standard deviation of 1.6%. The detection limit for carbamazepine is approximately 2 ng/ml, requiring 1 ml of plasma.