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941.
Marlin Opałło Nagao Kobayashi Tetsuo Osa 《Journal of inclusion phenomena and macrocyclic chemistry》1989,7(4):413-422
The complexation of 2,3-anthracenedicarboxylate (ADC) by- and-cyclodextrins in water containing an organic solvent has been studied by induced circular dichroism. It has been shown that an increase of organic solvent ratio causes the degradation of the 1:1 ADC:-CD complex and the liberation of one guest molecule from the 2:1 ADC:-CD complex in water. The higher the hydrophobicity of the cosolvent, the weaker the complexation of ADC by-CD. 相似文献
942.
(tBuC5H4 ) 2 MCl2 (M =Ti(1a) ,Zr(1b) ,Hf(1c) )和 (tBu2 C5H3 ) 2 MCl2 (M =Ti(2a) ,Zr(2b) ,Hf(2c) )可以通过单叔丁基环戊二烯基锂或双叔丁基环戊二烯基锂与MCl4 (M =Ti,Zr,Hf)在四氢呋喃中反应制备得到 ,用IR、1H NMR和EI MS对这些化合物进行了表征 .采用X光单晶结构分析测定了 (tBuC5H4 ) 2 HfCl2 的晶体结构 .六个化合物均具有一定的催化乙烯聚合活性 相似文献
943.
牛心朴子草植物农药的化学成分与生物活性研究 总被引:16,自引:0,他引:16
在分离鉴定化学组分基础上结合普筛农药活性,发现牛心朴子草提取物中生物碱部位显示抗植物病毒极高活性。通过生物活性跟踪与色谱分离、结构鉴定,确定它是菲并吲哚里西啶生物碱,包括7-脱甲氧基娃儿藤碱(Antofine)(1)和N-氧代-7-脱甲氧基娃儿藤碱(N-Oxideantofine)(2)。其中2是首次从该草分离得到。Antofine(1)是该草抑制植物病毒主要成份;半中枯斑法测定它在10^-^6g/mL浓度的枯斑抑制率达60%,比对照的常用植物病毒抑制剂活性高1~2个数量级。用多种生测方法验证该草生物碱试样抗植物病毒如烟草花叶病毒(TMV)、马铃薯Y病毒(PVY)、芜菁花叶病毒(TuMV)等的生物活性。 相似文献
944.
在常温下制备了具有不同钛含量的大比表面积和孔体积的介孔分子筛HMS.XRD谱表明,这些Ti-HMS样品呈现出很好的六方晶形.经焙烧后,Ti-HMS样品的UV吸收光谱和XAFS谱结果表明,在Ti-HMS(1)和Ti-HMS(2)骨架中的钛离子以四配位存在,而在Ti-HMS(10)中至少有部分钛是以六配位存在.在NO存在的情况下,在273K下光催化剂Ti-HMS受紫外光照射后,导致NO分解生成N2,O2和N2O.实验结果表明,具有高分散四配位钛的Ti-HMS(1)使NO以高效率、高选择性分解生成N2和O2;随着钛含量的增加,其光催化活性反而降低. 相似文献
945.
Efficient synthesis of cyclic -alkyl--dicarbonyl compounds of the cyclopentane, cyclohexane, tetronic acid, and -pyrone series from the corresponding cyclic -acyl--dicarbonyl compounds under the action of NaBH3(CN) in a THF--HCl system is described. 相似文献
946.
V. M. Timoshenko Ya. V. Nikolin A. N. Chernega E. B. Rusanov Yu. G. Shermolovich 《Chemistry of Heterocyclic Compounds》2001,37(4):470-476
The reaction of 1,1-dihydropolyfluoroalkyl benzyl sulfones with sodium azide or trimethylsilyl azide in the presence of tertiary amines gives ammonium salts of 4-benzylsulfonyl-5-polyfluoroalkyl--triazoles. The proposed reaction scheme includes the participation of catalytic amounts of azide ion in the cyclization of the formed intermediate vinyl azides to triazoles. X-ray analysis of 1,4-diazabicyclo[2.2.2]octane salt of 4-benzylsulfonyl-5-(-H-hexafluoropropyl)--triazole has been carried out. 相似文献
947.
948.
The antitumor prodrug temozolomide (TMZ) decomposes in aqueous medium of pH≥7 but is relatively stable under acidic conditions. Pure TMZ is obtained as a white powder but turns pink and then brown, which is indicative of chemical degradation. Pharmaceutical cocrystals of TMZ were engineered with safe coformers such as oxalic acid, succinic acid, salicylic acid, d,l ‐malic acid, and d,l ‐tartaric acid, to stabilize the drug as a cocrystal. All cocrystals were characterized by powder X‐ray diffraction (PXRD), single crystal X‐ray diffraction, and FT‐IR as well as FT‐Raman spectroscopy. Temozolomide cocrystals with organic acids (pKa 2–6) were found to be more stable than the reference drug under physiological conditions. The half‐life (T1/2) of TMZ–oxalic and TMZ–salicylic acid measured by UV/Vis spectroscopy in pH 7 buffer is two times longer than that of TMZ (3.5 h and 3.6 h vs. 1.7 h); TMZ–succinic acid, TMZ–tartaric acid, and TMZ–malic acid also exhibited a longer half‐life (2.3, 2.5, and 2.8 h, respectively). Stability studies at 40 °C and 75 % relative humidity (ICH conditions) showed that hydrolytic degradation of temozolomide in the solid state started after one week, as determined by PXRD, whereas its cocrystals with succinic acid and oxalic acid were intact at 28 weeks, thus confirming the greater stability of cocrystals compared to the reference drug. The intrinsic dissolution rate (IDR) profile of TMZ–oxalic acid and TMZ–succinic acid cocrystals in buffer of pH 7 is comparable to that of temozolomide. Among the temozolomide cocrystals examined, those with succinic acid and oxalic acid exhibited both an improved stability and a comparable dissolution rate to the reference drug. 相似文献
949.
Basi V. Subba Reddy Nagendra Nath Yadav Nikhil Srivastava Jhillu S. Yadav Balasubramanian Sridhar 《Helvetica chimica acta》2012,95(1):76-86
Ionic liquids were found to be a suitable reaction medium for 1,4‐dipolar cycloaddition reactions of an isoquinoline, an activated alkyne, and a 4‐oxo‐4H‐1‐benzopyran‐3‐carboxaldehyde at room temperature to afford [1]benzopyrano‐pyrido‐isoquinoline (=9aH,15H‐benzo[a][1]benzopyrano[2,3‐h]quinolizine) derivatives selectively in good yields. The ionic liquid can be recovered and recycled in further runs without loss of activity. 相似文献
950.
Several 2‐alkylquinolizinium‐1‐olates 9 , i.e., heterobetaines, were prepared from ketone 11 , the latter being readily available either from pyridine‐2‐carbaldehyde via a Grignard reaction, followed by oxidation with MnO2, or from 2‐picolinic acid (=pyridine‐2‐carboxylic acid) via the corresponding Weinreb amide and subsequent Grignard reaction. Mesoionic heterobetaines such as quinolizinium derivatives have the potential to undergo cycloaddition reactions with double and triple bonds, e.g., 1,3‐dipolar cycloadditions or Diels? Alder reactions. We here report on the scope and limitations of cycloaddition reactions of 2‐alkylquinolizinium‐1‐olates 9 with electron‐poor acetylene derivatives. As main products of the reaction, 5‐oxopyrrolo[2,1,5‐de]quinolizines (=‘[2.3.3]cyclazin‐5‐ones’) 19 were formed via a regioselective [2+3] cycloaddition, and cyclohexadienone derivatives, formed via a Diels? Alder reaction, were obtained as side products. The structures of 2‐benzylquinolizinium‐1‐olate ( 9a ) and two ‘[2.3.3]cyclazin‐5‐ones’ 19i and 19l were established by X‐ray crystallography. 相似文献