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91.
Dr. Ji-Rong Huang Dr. Muhammad Sohail Dr. Tohru Taniguchi Prof. Dr. Kenji Monde Prof. Dr. Fujie Tanaka 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2017,129(21):5947-5951
Spiro[4,5]decanes and polycyclic compounds bearing spiro[4,5]decane systems are important biofunctional molecules. Described are diastereoselective formal (4+1) cycloaddition reactions to afford oxindole-functionalized spiro[4,5]decanes and organocatalytic enantioselective Michael–Henry cascade reactions of the (4+1) cycloaddition products to generate spirooxindole polycyclic derivatives bearing the spiro[4,5]decane system. Spiro[4,5]decanes bearing oxindoles containing three stereogenic centers and spirooxindole polycycles having seven stereogenic centers, including two all-carbon chiral quaternary centers and one tetrasubstituted chiral carbon center, were obtained with high diastereo- and enantioselectivities. 相似文献
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We propose a new scheme for the coherent control of birefringent light pulses propagation in a four-level atomic medium. We modify the splitting of a light pulse by controlling the electric and magnetic responses. The Doppler broadening effect is also noted on the propagation of the birefringent pulses. The dispersions of the birefringence beams are oppositely manipulated for delay and advancement of time at a Doppler width of 10γ. A time gap is created between the birefringence beams, which protects from hacking of information. The time gap is then closed to restore the pulse into the original form by a reverse manipulation of the dispersion of the birefringence beams, i.e., introducing another medium whose transfer function is the complex conjugate of that of the original medium. The results are useful for secure communication technology. 相似文献
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Mohammad Javad TAGHIZADEH Maryam Saleh MOHAMMADNIA Masoumeh GHALKHANI Esmail SOHOULI 《高等学校化学研究》2022,38(2):546-551
Azaperone, with anti-anxiety and anti-aggressive activities used in veterinary medicine, is a member of the butyrophenone class. It is ordinarily utilized for a wide range of indications, such as sedation, obstetrics, and anesthesia. In this research, an improved synthetic route is presented for azaperone using a phase-transfer catalyst(PTC). In general, it was synthesized as a dopamine antagonist in four steps. The bis(2-chloroethyl) amine intermediate is easily obtained after the conversion of the alcohol groups into the chloride leaving group using thionyl chloride(95% yields). The alkylation of commercially available 2-amino pyridine in the presence of PTC was then carried out, giving 1-(pyridin-2-yl) piperazine with 75% yield. 1-(Pyridin-2-yl) piperazine was finally alkylated using 4-chloro-1-(4-fluorophenyl) butan-1-one to achieve azaperone with 60% yield. The butyrophenone intermediate was obtained via the Friedel-Crafts reaction of fluorobenzene with 4-chlorobutyryl chloride in the presence of AlCl3. High efficiency, gentle reaction conditions, and fast and simple procedure are the advantages of this method. Also, the electrochemical oxidation behaviour of azaperone was investigated using cyclic and differential pulse voltammetry techniques. Cyclic voltammetric studies indicated an irreversible process for azaperone electro-oxidation with a peak potential of 0.78 V in a phosphate buffer solution(pH=7.0) vs. Ag/AgCl(saturated KCl) electrode. The value of the peak current vs. the azaperone concentration was enhanced linearly in the range of 10―70 μmol/L, and the detection limit was found to be 3.33 μmol/L. 相似文献
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