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61.
Xiao-Qiang Dai Wen-Xiu Xu Ya-Long Wen Xing-Hai Liu Jian-Quan Weng 《Tetrahedron letters》2018,59(30):2945-2949
Metal and acid-free visible light-induced Friedel-Crafts C3-alkylation reactions of indole derivatives were developed using N,N-dimethylanilines as the carbon source. A cheap and readily available organic dye, Rose Bengal, was applied as the photocatalyst. This environmentally friendly transformation afforded C3-alkylated indoles in moderate to good yields under mild conditions. 相似文献
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Science China Chemistry - Supporting Pd catalysts characterized significant different size distribution were obtained using PdCl2, [Pd(NH3)4](NO3)2 and Pd(acac)2 as precursors. High-resolution... 相似文献
65.
Pao-Shu Chang Chien Chung Lig-Ji Yuan Pao-Shan Weng 《Journal of Radioanalytical and Nuclear Chemistry》1985,92(2):343-356
This work describes a nuclear facility forin vivo prompt gamma activation analysis (IVPGAA) using a moderated neutron beam from a 0.1 W Tsing-Hua Mobile Educational Reactor (THMER). The IVPGAA measurement is a new technique for toxic cadmium determination in organs, which can efficiently be used in clinical diagnosis. The low-power nuclear reactor provides a total neutron flux of 3.3·104 n·cm–2·s–1 on the surface of the central vertical neutron beam tube to which a liquid phantom is positioned. The capability of such partial-body irradiation facility is demonstrated. The detection limit of cadmium in the left kidney for a skin dose equivalent of 1.66 mSv (166 mrem) was 1.34 mg in a 500-s irradiation/counting period, and the sensitivity in the left kidney was 103 counts mg–1·mSv–1. The performance of IVPGAA system using the THMER nuclear facility therefore has the advantages of mobility and feasibility with high sensitivity under low neutron and gamma doses. 相似文献
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反相高效液相色谱法测定尿中吡啶醚和脱氧吡啶醚 总被引:13,自引:0,他引:13
尿中吡啶醚(pyridinoline,PYD)和脱氧吡啶醚(deoxypyridinoline,DPD)是骨代谢特异的生化指标。应用高效液相色谱法(HPLC)建立了尿中PYD和DPD的测定方法。尿液用6mol/LHCl水解后,以纤维素CF1小柱提取,然后用HPLC测定;色谱系统为SpherisorbC18反相色谱柱,流动相组成为15%甲醇添加0.1%七氟丁酸,流速为1.2mL/min。系统的检测限:PYD为10nmol/L,DPD为7nmol/L;回收率:PYD为91.5%,DPD为106.1%;日内变异 相似文献
69.
Seik Weng Ng V. G. Kumar Das Jaroslav Hole
ek Antonin Ly
ka Marcel Gielen Michael G. B. Drew 《应用有机金属化学》1997,11(1):39-45
Bis(dicyclohexylammonium) bis(2,6-pyridinedicarboxylato)dibutylstannate is assigned seven-fold coordination at tin on the basis of its 119Sn CP/MAS NMR chemical shift (δ=−424.9 ppm). The assignment has been corroborated by a crystal structure determination of its monohydrate, whose tin atom has the trans -C2SnNO4 pentagonal bipyramidal [Sn–C=2.040(9), 2.067(8) Å; C–Sn–C =168.9(5)°] geometry. One 2,6-pyridine- dicarboxylato group chelates to the tin atom (Sn–O=2.234(4), 2.260(4); Sn–N =2.279(5) Å) whereas the other binds through only one carboxyl –CO2 end (Sn–O=2.416(5), 2.441(5) Å). Hydrogen bonds link the cation and the stannate into a linear chain parallel to the b -axis. The lattice water molecule is hydrogen-bonded to the free carboxyl end. The anhydrous compound showed higher in vitro antitumor activity than those of carboplatin and cisplatin when screened against breast (MCF-7, EVSAT), colonic (WiDr), ovarian (IGROV) and renal (A498) carcinoma, and melanoma (M19 MEL) cell lines. © 1997 by John Wiley & Sons, Ltd. 相似文献
70.
Qiang Cheng Jia‐Hao Xie Yue‐Cheng Weng Shu‐Li You 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(17):5795-5799
Dearomatization of anthranils with vinylcyclopropanes (VCPs) by Pd‐catalyzed [4+3] cyclization reaction has been realized. In the presence of a catalytic amount of borane as an activator, bridged cyclic products were obtained in good to excellent yields with excellent stereoselectivities. By introducing a chiral PHOX ligand ( L5 ), asymmetric dearomatization reactions of anthranils with vinylcyclopropanes proceeded with excellent enantioselectivity. Borane plays a key role for the reactivity, likely owing to the formation of a borane–anthranil complex which has been confirmed by NMR experiments. 相似文献