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991.
A single isomer of a monofunctionalised C70 fullerene is isolated and characterised using variable temperature NMR spectroscopy. Pendant methylene bromide groups allow for further cycloaddition reactions and a C60-C70 asymmetric fullerene dimer is thus prepared.  相似文献   
992.
The anti-Parkinson’s agent SIB-1508Y was prepared in six steps from (S)-nicotine in 20% overall yield. The strategy involves a regioselective formylation at C-5 of a 1,4-dihydronicotine intermediate.  相似文献   
993.
The synthesis of chiral oxazolidinedione derived bicalutamide analogs has been discussed.  相似文献   
994.
995.
Specific features of the formation of local and statistical polarization structures of laser radiation scattered in phase-inhomogeneous layers (PIL) of biological tissue (BT) were studied. The distribution of azimuth and eccentricity of boundary field polarization was found to correlate with the orientation-phase structure of multifractal PIL. A method of polarization phase reconstruction of BT architectonics was suggested.  相似文献   
996.
It is pessible to study experimentally Cherenkov light spectra in a liquid scintillation spectrometer with colour filters. Cherenkov light spectra of60Co,198Au,115Cd,143Ce,140La,32P,86Rb,76As,42K and an external standard were studied in a Packard 3375 type liquid scintillation spectrometer, using 11 various Kodak Wratten filters. The absorption maxima of the filters ware in the 410–796 nm interval.  相似文献   
997.
In this paper, we report on the design and optical properties of laser diodes with an emission wave-length of ~1170 nm based on an (InGa)As/GaAs double quantum well active layer. The back and front facet of the laser diodes were coated with SiOx dielectric films that influence the output optical power by enhancing or lowering the facet reflectivity. The measurements show improvement of the facet-coated laser diode properties in the threshold-current-density reduction along with light output power enhancement. Furthermore, a narrow far field pattern and high side mode suppression have been observed.  相似文献   
998.
999.
Peptidosulfonamides are an emerging group of peptidomimetics with a variety of applications in medicinal chemistry. We present a novel approach to the synthesis of peptidosulfonamides, and apply it to a series of new potential inhibitors of the bacterial peptidoglycan biosynthesis enzymes MurD and MurE. The synthesis was conducted via N-phthalimido β-aminoethanesulfonyl chlorides, which are new building blocks for the synthesis of peptidosulfonamides. In the most crucial step, sulfonic acids or their sodium salts were converted into the corresponding sulfonyl chlorides using an excess of either SOCl2 or SOCl2/DMF, and then coupled to the C-protected amino acid. None of the compounds significantly inhibited MurD, however, some inhibited MurE; one had an IC50 below 200 μM, which constitutes a promising starting point for further development. Molecular modelling simulations were performed on two analogues to investigate the absence of inhibitory activity of the sulfonamide compounds on MurD.  相似文献   
1000.
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