Novel enhancement of the reducing ability of ytterbium diiodide by irradiation with near-UV light

Irradiation with near-UV light, dramatically enhances the reducing ability of ytterbium diiodide (YbI₂). Organic bromides, iodides, tosylates, and tellurides are reduced efficiently by a YbI₂-hv system, while these can not be reduced with YbI₂ in the dark.     

Exciton and magneto-absorption in tellurium

Infrared magneto-absorption has been investigated in tellurium crystals in magnetic fields up to 45 koe at liquid helium temperatures. When the magnetic field was applied parallel or perpendicular to the c-axis, oscillatory absorptions with many transmission minima involving the exciton absorption were observed. The results were analysed taking into account the complicated structure of the valence band.     

Stereospecific synthesis of chiral precursors of thienamycin from L-Threonine

L-Threonine was transformed, stereospecifically, to a versatile β-lactam (5a) in 3 steps. This β-lactam was further converted to a key intermediate (25) for the synthesis of thienamycin and its biologically active analogues. Furthermore, the compound 5a was changed to iodides (18 and 23), cyanides (19 and 24), chloromethylketone (26) and aldehydes (30 and 31) which appear to have a latent potential as precursors for the syntheses of the carbapenems.     

The structure of arugomycin,a new anthracycline antibiotic part I. structural elucidation of degradation products,AG1, AG2 and AG3.

Based on ¹H- and ¹³C-NMR and mass spectral analysis and chemical degradation, the structures of degradation products of arugomycin (arugorol, AG1, AG2 and AG3) have been determined as shown in Fig. 1.     

A new synthesis of olefins. Conversion of nitroolefins into olefins by reductive elimination

A nitro group in nitroolefins is displaced by hydrogen giving the corresponding olefins in good yields by the reaction of nitroolefins with sodium sulfide in the presence of benzenethiol. It proceeds rapidly at room temperature.     

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