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1.
O. V. Shablykina O. V. Khilya V. V. Ishchenko V. P. Khilya 《Chemistry of Natural Compounds》2005,41(5):529-532
3-(2-Quinolyl)- and 3-(5-carbethoxyfuryl-2)coumarins were prepared by reaction of substituted salicylaldehydes and hetarylacetonitriles.
Alkylation and acylation of 3-hetaryl-7-hydroxycoumarins were studied.
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Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 432–434, September–October, 2005. 相似文献
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O. V. Khilya O. V. Shablykina M. S. Frasinyuk V. V. Ishchenko V. P. Khilya 《Chemistry of Natural Compounds》2005,41(5):523-528
3-(2-Pyridyl)coumarins were prepared by reaction of substituted salicylaldehydes and 2-pyridylacetonitrile. Benzylation, acylation,
and aminomethylation of 7-hydroxy-3-(2-pyridyl)coumarin was studied.
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Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 428–431, September–October, 2005. 相似文献
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On the Structure of Sr3(BN2)2 The structure of Sr3(BN2)2 was determined on single-crystal X-ray data collected with a four-circle diffractometer. Sr3(BN2)2 crystallizes in the cubic space group Im3 m (no. 229) with a = 764.56(3) pm and Z = 3. The structure contains linear BN3?2 ions with a B? N bond length of 135.8(6) pm. The straight forward synthesis employing metal nitrides plus boron nitride yielded crystalline powders of M3(BN2)2 (M = Ca, Sr) at 1100°C (5 days). Cubic indexing of guinier patterns gave a = 765.8(1) pm for M = Sr and a = 734.7(2) pm for M = Ca. The structure refinement on a single crystal of Sr3(BN2)2 revealed that one strontium site (2a; 0, 0, 0) is occupied by only about 50%. It has been tried to fully occupy this site with an alkali metal (A) to obtain ASr4(BN2)3 (Z = 2). Reactions with A = Na yielded crystalline powders. Cubic indexing of the guinier pattern analogous to that of Sr3(BN2)2 gave a = 754.2(1) pm. 相似文献
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3-Chloro-2-polyfluoroalkyl- and 3-chloro-6-nitro-2-polyfluoroalkylchromones were synthesized. These compounds react with N2H4·2HCl on boiling in ethanol to form 4-chloro-3(5)-(2-hydroxyaryl)-5(3)-polyfluoroalkylpyrazoles. 相似文献
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O. V. Khilya O. V. Shablykina M. S. Frasinyuk A V. Turov V. V. Ishchenko V. P. Khilya 《Chemistry of Heterocyclic Compounds》2004,40(11):1408-1420
3-(2-Thiazolyl)coumarins were obtained by the reaction of substituted salicylaldehydes with 2-thiazolylacetonitriles. Methylation, acylation, and aminomethylation were studied for the 7-hydroxy-substituted products.For Communication 1, see [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1632–1644, November, 2004. 相似文献
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V. T. Abaev M. G. Kadieva A. V. Butin G. D Krapivin E.T. Oganesyan V. E. Zavodnik 《Chemistry of Heterocyclic Compounds》2000,36(11):1261-1271
Methods were developed for the synthesis of 3-butyl-2-(3-oxobutenyl)benzofurans and 3-(3-furylbenzofuran-2-yl)acrylic acids on the basis of 3-furyl-2-(3-oxobutyl)benzofurans. 相似文献
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采用高温固相法合成了Ce3+,Tb3+掺杂激活的CaBa2(BO3)2荧光粉,并对其发光特性进行了研究。观察到CaBa2(BO3)2中Ce3+对Tb3+发光的敏化现象。在367 nm紫外光激发下,单掺Tb3+时CaBa2(BO3)2不发光。当Ce3+和Tb3+共掺时,出现Tb3+的发射峰,样品发绿光,表明Ce3+对Tb3+的发光有很强的敏化作用。根据Forster-Dexter理论,分析Ce3+和Tb3+的能量传递过程,还证明在CaBa2(BO3)2:Ce3+,Tb3+中Ce3+对Tb3+的能量传递属于共振能量传递。 相似文献
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Anthranilonitrile reacting with formic acid at room temperature for three days gave 64% of 3-(2-cyanophenyl)quinazolin-4(3H)-one. Under similar conditions anthranilic acid. 4-nitroaniline, and 2,5-dichloroaniline were N-formylated in good yields.Institute of Organic Chemistry and Technology, Silesian Technical University, Krzywoustego, 4, 44–100 Gliwice, Poland; e-mail: wojtex@zeus.polsl.gliwice.pl. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 922–924, July, 2000. 相似文献
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The Synthesis of 3-(2'-Hydroxybutyl) isobenzofuran-1 (3H)-one 总被引:1,自引:0,他引:1
l(3H】.Isobenzoturans(Dhthalldes】werereDortedtoexhibitawiderangeofbiologicalactivities.Forexample,3-n-butylphthallde(NB)exhibitsantlasthmatlc’,antlconvuls-ant“actlvltles.PenEandZhouhavestudiedonthemetabolismofNBPInrats‘.Theyfoundthat... 相似文献
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JIANG Yinzhi & HU Weixiao . Department of Pharmaceutical Science Zhejiang University of Technology Hangzhou China . Department of Applied Chemistry Zhejiang Institute of Science Technology Hangzhou China 《中国科学B辑(英文版)》2004,47(3)
Rare earth complexes with organic ligands have been used as luminescence-material usually. Except their luminescent property, the complexes of trivalent lanthanide ions have low toxicity and powerful para-magnetic properties[1,2], so the lanthanide complexes are associated with important biological uses as diag-nostic tools and medicines[36]. Recently, there are some reports on Ce(III) complexes, some of which show anti-cancer activities[7]. S- tetrazines can be used as poly-dentate chelatin… 相似文献
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N. Yu. Gorobets A. V. Borisov A. V. Silin V. M. Nikitchenko S. N. Kovalenko 《Chemistry of Heterocyclic Compounds》2002,38(11):1389-1396
The reaction of 3-(4-aryl-2-thiazolyl)- and 3-(2-benzothiazolyl)-2-iminocoumarins with N-nucleophiles was studied. This reaction gives 2-N-substituted 3-(4-aryl-2-thiazolyl)- and 3-(2-benzothiazolyl)iminocourmarins. N-Nucleophiles such as arylamines, heterocyclic amines, and hydrazine derivatives undergo this reaction. 相似文献
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Synthesis and Structure of [(Ph3C6H2)Te]2, [(Ph3C6H2)Te(AuPPh3)2]PF6 and [(Ph3C6H2)TeAuI2]2 [(2,4,6-Ph3C6H2)Te]2 reacts with Ph3PAu+ to yield [2,4,6-Ph3C6H2TeAuPPh32]PF6 which can be oxidized by I2 to form the gold(III) complex [(2,4,6-Ph3C6H2)TeAuI2]2. [(2,4,6-Ph3C6H2)Te]2 crystallizes in the monoclinic space group P21/c with a = 810.6(2); b = 2026.5(5); c = 2260.6(7) pm; β = 99.23(3)° and Z = 4. In the crystal structure the ditelluride exhibits a dihedral angle C11? Te1? Te2? C21 of 66.1(2)°. The distance Te1? Te2 is 269.45(6) pm. In the cation of the triclinic complex [(2,4,6-Ph3C6H2)Te(AuPPh3)2]PF6 (space group P1 ; a = 1197.4(3); b = 1457.2(4); c = 1680.0(6) pm; α = 84.69(3)°; β = 85.11(3)°; γ = 75.54(3)°; Z = 2) a pyramidal skeleton RTeAu2 with distances Te? Au = 259.2(1) and 257.8(2) pm and Au? Au = 295.3(1) pm is present. [(2,4,6-Ph3C6H2)TeAuI2]2 crystallizes in the triclinic space group P1 with a = 1086.3(3); b = 1462.9(6); c = 1654.2(2) pm; α = 85.25(2)°; β = 87.44(1)°; γ = 80.90(3)°; Z = 2. In the centrosymmetrical dinuclear complex [(2,4,6-Ph3C6H2)TeAuI2]2 the Au atoms exhibit a square-planar coordination by two iodine atoms and two tellurolate ligands. The tellurolate ligands form symmetrical bridges with distances Te? Au = 260.0 pm. The distances Au? I are in the range of 260.3(1) and 263.7(1) pm. 相似文献
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V. O. Kozminykh D. B. Oborin V. I. Goncharov E. N. Kozminykh 《Chemistry of Heterocyclic Compounds》2007,43(8):978-980
3-Hydroxy-3-(2-oxoethyl)-6-phenyl-2,3-dihydropyridazin-4(1H)-ones were obtained by the reaction of methyl 3-oxo-5-phenylfuran-2(3H)-ylideneacetate
or 2-[2-(4-chlorophenyl)-2-oxoethylidene]-5-phenylfuran-3(2H)-one with benzoic or p-nitrobenzoic isopropylidenehydrazides.
Equilibrium C(5)H and C(5)H2 tautomeric forms were detected in solutions of the 4-chlorophenyl derivatives in DMSO-d6.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1156–1158, August, 2007. 相似文献
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本文主要用气相色谱逸出气体分析方法,借助于红外、紫外可见漫反射谱等手段研究了[Co(NH_3)_5(H_2O)]Br_3、[Cr(NH_3)_5(H_2O)](NO_3)_3与无机盐KY(Y=Cl,Br,Ⅰ)的固相反应,计算了失水与失氨的动力学参数,发现第一步反应失水生成一取代中间产物,其活化能与外加阴离子无关,为S_N1过程。第二步失氨反应活化能与中心离子M以及取代基Y有关,当M=Co(Ⅲ)时,反应体系的失氨活化能大小有下列顺序:Cl>Br>Ⅰ(E值分别为187、155、98kJ·mol~(-1)),M=Cr(Ⅲ)时则正好相反:Ⅰ>Br>Cl(E值分别为213、146、79 kJ·mol~(-1))。 相似文献
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Ralf Eßmann Guido Kreiner Anke Niemann Dirk Rechenbach Axel Schmieding Thomas Sichla Uwe Zachwieja Herbert Jacobs 《无机化学与普通化学杂志》1996,622(7):1161-1166
The Structures of some Hexaammine Metal(II) Halides of 3 d Metals: [V(NH3)6]I2, [Cr(NH3)6]I2, [Mn(NH3)6]Cl2, [Fe(NH3)6]Cl2, [Fe(NH3)6]Br2, [Co(NH3)6]Br2 and [Ni(NH3)6]Cl2 Crystals of yellow [V(NH3)6]I2 and green [Cr(NH3)6]I2 were obtained by the reaction of VI2 and CrI2 with liquid ammonia at room temperature. Colourless crystals of [Mn(NH3)6]Cl2 were obtained from Mn and NH4Cl in supercritical ammonia. Colourless transparent crystals of [Fe(NH3)6]Cl2 and [Fe(NH3)6]Br2 were obtained by the reaction of FeCl2 and FeBr2 with supercritical ammonia at 400°C. Under the same conditions orange crystals of [Co(NH3)6]Br2 were obtained from [Co2(NH2)3(NH3)6]Br3. Purple crystals of [Ni(NH3)6]Cl2 were obtained by the reaction of NiCl2 · 6H2O and NH4Cl with aqueous NH3 solution. The structures of the isotypic compounds (Fm3 m, Z = 4) were determined from single crystal diffractometer data (see “Inhaltsübersicht”). All compounds crystallize in the K2[PtCl6] structure type. In these compounds the metal ions have high-spin configuration. The orientation of the dynamically disordered hydrogen atoms of the ammonia ligands is discussed. 相似文献
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微波辐照下(Bi_2O_3)_(0.8)(La_2O_3)_(0.2)固熔体对甲烷氧化偶联的催化行为陈长林,洪品杰,戴树珊,阚家德(云南大学化学系,昆明,650091)关键词微波,甲烷氧化偶联,(Bi_2O_3)_(0.8)(La_2O_3)_(0.2)甲烷氧化... 相似文献
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Saeed Balalaie Hassan MotaghediMorteza Bararjanian Daryoush Tahmassebi Hamid Reza Bijanzadeh 《Tetrahedron》2011,67(47):9134-9141
An efficient method for the stereoselective synthesis of 3-(diarylmethylene)-2-oxindoles and 3-(arylmethylene)-2-oxindoles via carbopalladation is described. In this approach, an Ugi-4-component reaction (4-CR) adduct was used as the starting material. A one-pot sequence involving intermolecular carbopalladation C-H activation/C-C bond formation efficiently afforded the oxindole derivatives. 相似文献