13C-NMR and Molecular Orbital Studies of Protonation to Formanilides

The effect of protonation to formanilides was studied by measurements of ¹³C-NMR chemical shifts in CDCl₃ and methanesulfonic acid. It was found that the ¹³C shift of the ring carbon, to which the amide group is attached, exhibits an upfield shift by the protonation, whereas the peaks of the rest of ring carbons and carbonyl carbon shift downfield. The protonation-induced shifts of the ring carbons were found to be roughly correlated with the differences of the total electron densities between formanilides and their monocations. From the comparison between the protonation-induced shifts and the differences of the total electron densities at the carbons, especially at the carbonyl carbon, it is suggested that N-protonation is partly involved, although O-protonation seems to be dominant.     

Quark mixings in a subquark model

Quark mixings and theor momentum dependences are discussed in a subquark model in which the weak current is made of the iso-doublet spinor subquarks. The Cabibbo angle is predicted to become larger as momentum transfer between quarks grows up.     

High pressure study on the superconducting transition temperature and Hall coefficient of Ba1−xKxBiO3 up to 8 GPa

The superconducting transition temperature (T_c) of Ba_0.62K_0.38Bio₃ (T_c=30 K) has been measured under high pressure up to 8 GPa. It is observed that T_c increases initially with pressure, as reported by Uwe et al., Shirber et al. and Huang et al., but decreases above 4 GPa. The Hall coefficient of Ba_0.62K_0.38BiO₃ has been measured up to 1.2 GPa. The absolute value of the Hall coefficient decreases with pressure by 10% GPa, the value of which is almost the same as that obtained in most CuO-based high-temperature superconductors.     

Single-electron-capture cross sections for 0.4–5.0 keV He+ ions incident on alkali-vapor targets

Total cross sections for single-electron capture by He⁺ ions in vapor targets of Cs, Rb, K and Na have been determined in the energy range 0.4–5.0 keV. The energy dependence of the cross-section curves is very similar for all the targets. The cross sections for all the targets are maximum at about the same energy, 1.5 keV. Comparison is made with other reported experimental and theoretical results.     

Totalsynthetische untersuchungen an steroiden—VIII Einführung der C-substituenten in die angulare stellung der kondensierten ringsysteme (teil 3). Einwirkung von kaliumcyanid unter zusatz von ammoniumchlorid auf rac. D-homo-18-nor-androstanderivate

Durch Einwirkung von 2 Mol Kaliumcyanid und 1·75 Mol Ammoniumchlorid und nachträgliche Ketalisierung und Acetylierung liess sich rac. -Homo-18-nor-13(17a)-androstan-3β-ol-17-on (I) in die verschiedenen am C₁₃ cyanierten Verbindungen verwandeln. Das Bildungsverhältnis von 13β- zur 13-Cyanverbindung lag bei 5:3. Die räumlichen Strukturen aller hierbei erhaltenen Verbindungen wurden ermittelt. Die angeführten Reaktionsfolgen stellen eine neue Methode zur Einführung der angularen Substituenten dar und lieferten einen Anhaltspunkt zur Totalsynthese der normalen sowie der in 18-Stellung mit einer funktionellen Gruppe versehenen Steroide.     

Synthetic studies on β-lactam antibiotics. VII. Mild removal of the benzyl ester protecting group with aluminum trichloride

The benzyl ester protecting group in β-lactam derivatives can be cleanly removed by treatment with aluminum trichloride under mild conditions, preferably in the presence of anisole, to give the corresponding free acids in high yields.     

Synthetic studies on β-lactam antibiotics. 15. conversion of 7-epicephems into 1-oxacephems

7-Epi-1-oxacephem was obtained by stereospecific, intramolecular etherification of alcohol prepared from 7-epicephems via aldehyde or formate. Synthesis of the 3-acetoxymethyl analogwas unsuccessful. Biologically active 1-oxacephems were derived from by known processes.