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971.
本文报道以3α-羟基-6-羰基-5α-胆烷酸甲酯(3)为原料经六步反应合成了油菜甾醇类似物25,26,27-三失碳-B-高-7-氧-6-酮-5α-胆甾-3α,24-二醇(9a).总产率14%.9a的促进植物生长作用是24-表油菜甾醇内酯的60%.  相似文献   
972.
Improved separations of the isomers of olefinic aliphatic insect pheromones were obtained on cholesteryl cinnamate glass capillary columns by operating in the supercooled temperature range of the liquid crystal. Capillary columns were prepared with varying film thickness of the stationary phase; choice of the correct film thickness ensured optimum retention for a wide range of compounds within the most effective temperature range of the liquid crystal. The deactivation procedures described made the liquid crystal columns suitable for separation of the geometric isomers of polar and nonpolar compounds.  相似文献   
973.
Mean amplitudes of vibration for various octahedral complex compounds of the typeLnCl6 3– andLnBr6 3– (withLn=Nd, Eu, Gd, Dy, Er, and Yb) have been calculated, at different temperatures, using known spectroscopic data. The results are briefly discussed and it is found that theLn–Cl andLn–Br amplitude values are highly characteristic.
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974.
A detector for HPLC is based on suppression of chemiluminescence from the Cu(II)-luminol-peroxide reaction. Analytes which complex Cu(II) reduce the free Cu(II) concentration and thus the observed chemiluminescence intensity. The degree of chemiluminescence suppression is a measure of the analyte concentrations. Detection limits are in the range of 1 pmole-1 nmole for amino acids (both primary and secondary without derivatization), CN, amines, catecholamines, catechol, and aminoglycoside antibiotics. The detection approach is demonstrated with an ion-exchange separation of amino acids, a reverse phase separation of catecholamines, and an ion-pair separation of the three components of gentamicin C in commercial gentamicin sulfate.  相似文献   
975.
The reaction ofn-hexylamine withO-alkylO-4-nitrophenyl chloromethylphosphonates in toluene solutions of poly(ethylene glycol)-600 monolaurate (PM) has been studied by spectrophotometry. The reverse micelles of the nonionic surfactant increase more than tenfold the observed rate constant of aminolysis. The catalytic activity of the surfactant is practically independent of the alkyl radical length of phosphonate. An increase in the concentration of amine results in a decrease in the catalytic efficiency. The character of the dependence of the rate constant on the concentration of PM is affected by the alkyl chain length of the substrate. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1735–1738, September, 1998.  相似文献   
976.
The molecular structure of 1,3,5-tris (trimethylstannyl) benzene has been determined by gas-phase electron diffraction. The C — C bond length is in good agreement with that in benzene. In agreement with the somewhat electron-releasing character of the substituents, the endocyclic bond angles at the substituents are somewhat smaller than 120°. The mean value of Sn — C bond lengths is greater than that in tetraphenyltin and tetramethyltin. The SnMe3 groups appear freely rotating around the Caryl — Sn bonds. The following bond lengths (r g) and bond angles were determined: (Sn — C)mean 2.150 ± 0.007 Å, C — C 1.399 ± 0.005 Å, (C — H)mean 1.105 ± 0.006 Å, < C — C(Sn) — C 117.7 ± 1.7º, < Caryl — Sn — Cmethyl 106.7 ± 0.7º < Sn — C — H 111.5 ± 0.9º.  相似文献   
977.
    
Ohne Zusammenfassung
Analytical importance of electron-impact induced retro-diels-alder reactions for stereochemical investigations
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978.
High temperature liquid water (HTLW), as an environmentally benign medium, has drawn increasing attention for organic chemical reactions and biomass conversion1-3. HTLW has a strong tendency to ionize and can act as an acid and/or base catalyst. In addition, HTLW can dissolve organic compounds to some extent allowing for a homogenous reaction within an aqueous phase. Extensive researches4-10 have been pursued on acid/base-catalysis reactions in HTLW without addition of acid or base. Howe…  相似文献   
979.
The kinetics of the oxidation of five catecholamines viz., dopamine (A), L-dopa (B), methyldopa (C), epinephrine (D) and norepinephrine (E) by sodium N-chloro-p-toluenesulfonamide or chloramine-T (CAT) in presence of HClO4 was studied at 30±0.1 °C. The five reactions followed identical kinetics with a first-order dependence on [CAT] o , fractional-order in [substrate] o , and inverse fractional-order in [H+]. Under comparable experimental conditions, the rate of oxidation of catecholamines increases in the order D>E>A>B>C. The variation of ionic strength of the medium and the addition of p-toluenesulfonamide or halide ions had no significant effect on the reaction rate. The rate increased with decreasing dielectric constant of the medium. The solvent isotope effect was studied using D2O. A Michaelis-Menten type mechanism has been suggested to explain the results. Equilibrium and decomposition constants for CAT-catecholamine complexes have been evaluated. CH3C6H4SO2NHCl of the oxidant has been postulated as the reactive oxidizing species and oxidation products were identified. An isokinetic relationship is observed with β=361 K, indicating that enthalpy factors control the reaction rate. The mechanism proposed and the derived rate law are consistent with the observed kinetics.  相似文献   
980.
制备了酸性磷酸酶检测底物2,6-二氯-4-乙酰基苯基磷酸酯(DCAP-P)。以2,6-二氯苯酚为原料,经酰化反应、AlCl3催化F-C重排、碱化成盐、磷酯化、水解等5步反应,制备了DCAP-P,并对F-C重排、磷酯化条件进行了改进。  相似文献   
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