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101.
T. V. Beryozkina N. N. Kolos V. I. Musatov V. D. Orlov 《Russian Chemical Bulletin》2006,55(6):1056-1059
3,4-Dihydrobenzo-1,4-oxazin-2-ones were obtained from the corresponding β-aroylacrylic acids and 2-aminophenols. With 2-amino-4(5)-nitrophenols,
stable intermediate β-amino adducts (4-aryl-4-oxobutyric acid derivatives) were isolated.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1018–1021, June, 2006. 相似文献
102.
T. V. Chernenko N. T. Ul'chenko A. I. Glushenkova 《Chemistry of Natural Compounds》2005,41(5):499-500
The quantitative composition of glycolipids from leaves of Eminium Lehmanii (Araceae) was established. It was shown that the predominant glycolipids were monogalactosyldiglycerides and digalactosyldiglycerides.
The fatty-acid compositions of six glycolipids, of which digalactosyldiglycerides and sterylglycoside esters contained greater
than 70% linoleic acid, were determined by GC. The main carbohydrate component of the leaf glycolipids was galactose.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 409–410, September–October, 2005. 相似文献
103.
V. P. Feshin M. Yu. Kon'shin A. V. Radushev E. V. Feshina V. Yu. Gusev A. E. Lesnov V. I. Karmanov 《Russian Chemical Bulletin》1996,45(11):2505-2508
The basicity of hydrazides of the highest aliphatic carboxylic acids RC(O)NHNH2 (R = CnH2n+1,n = 5-12) has been studied by potentiometric titration, and IR and1H NMR spectroscopy.Ab initio Hartree-Fork calculations using the 6–31G* basis set with full optimization of geometry were carried out on the simplest acy1hydrazines and their possible protonated forms. Based on these calculations, and the 1R and1H NMR spectra, the tautomerism of alkylhydrazides and the structures of their protonated forms are discussed.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2645–2649, November, 1996. 相似文献
104.
Fourier transform infrared reflection-absorption spectroscopy (FT-IRAS) has been used to study the orientation and coordination of glycine, L-phenylalanine and L-histidine on gold and copper surfaces. It was found that glycine and L-histidine were weakly adsorbed (physisorbed) in the zwitterionic form on gold. The surface chemical bonding of L-histidine and L-phenylalanine to copper were chemical rather than physical by nature. Conclusive evidence was obtained for coordination to copper through both the amino-nitrogen and carboxylate-oxygen atoms. 相似文献
105.
Viroids: a class of subviral pathogens 总被引:13,自引:0,他引:13
106.
Far-IR absorption and reflection spectra, as well as laser Mandelshtam–Brillouin and Raman scattering spectra of -glycine, β-alanine,
-histidine,
-tryptophane single crystals in the 0.2–400 cm−1 range were investigated. It was revealed that the far-IR and Raman spectra of the amino acids under study contain more bands than predicted by factor-group analysis, thus indicating a possible contribution of low-energy intramolecular vibrations and overtones, as well as an emergence of forbidden vibrations. Some of the low-frequency bands have never, to our knowledge, been detected previously. 相似文献
107.
A. V. Orlinkov T. V. Chulochnikova A. I. Nesmelov V. B. Murachev E. A. Ezhova A. M. Evtushenko 《Russian Chemical Bulletin》1996,45(5):1124-1127
The effects of the nature of halogens in the initiatingtert-butyl halide-aluminum-containing Lewis acid system on the number average molecular weightM
n
and the structure of end groups of polyisobutylene macromolecules obtained in the cationic polymerization of isobutylene in hexane at -78 °C were studied. An increase inM
n
is observed in the transition from chlorine to bromine and iodine, accompanied by a decrease in the fraction of end C=C groups and an increase in the relative content of C-Hal groups (Hal = Cl, Br, and I). When atoms of different halogens are present in the counterion, more bulky atoms preferentially participate in the formation of the end groups. The results are interpreted within the framework of the principle of hard and soft acids and bases.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 1184–1187, May, 1996. 相似文献
108.
建立了使用超高效液相色谱-串联质谱(UHPLC-MS/MS)高效、快速直接测定茶叶中游离氨基酸的方法。通过对质谱、色谱条件及氨基酸提取条件的优化,以含0.2%(体积分数)甲酸的5 mmol/L乙酸铵水溶液和甲醇为流动相进行梯度洗脱,在电喷雾离子(ESI)源正离子扫描模式下检测,通过UHPLC-MS/MS测定,共解析了茶叶中的20种氨基酸。结果表明,茶氨酸(Thea)、Arg、Asn和Asp在50~500 μg/L范围内线性关系良好,其他氨基酸在10~250 μg/L范围内线性关系良好,相关系数均大于0.99;加标回收率为92.3%~109.2%,相对标准偏差为2.00%~9.88%,检出限为0.001~0.011 mg/L,定量限为0.010~0.053 mg/L。该方法灵敏、准确,具有良好的重复性和稳定性,可有效检测出茶叶中的20种氨基酸及氨基类成分。 相似文献
109.
A Taylor dispersion tube has been used to measure mutual diffusion in aqueous solutions of glycine hydrochloride at 25°C and concentrations from 0.0005 to 0.5 M. Analysis of the dispersion profiles shows that the diffusion of glycine hydrochloride (GlyHCl) produces a subtantial additional flow of hydrochloric acid that is liberated by the dissociation: GlyH+ + Cl- Gly + H+ + Cl-. Diffusion in this system is, therefore, a ternary process described by the equations J
1(GlyHCl) = – D
11C
1 – D
12C
2 and J
2(HCl) = –D
21C
1 – D
22C
2 for the coupled fluxes of total glycine hydrochloride (1) and hydrochloric acid (2) components. The ratio D
21/D
11 of measured diffusion coefficients indicates that up to two moles of HCl are cotransported per mole of GlyHCl. Although protonated glycine diffuses with relatively mobile Cl– counterions, the main diffusion coefficient of glycine hydrochloride, D
11, is lower than or nearly identical to the diffusion coefficient of aqueous glycine. A model for the diffusion of protonated solutes is developed to interpret this result and the large coupled flows of HCl. Diffusion coefficients are also reported for the aqueous hydrochlorides of 3- and 4-aminobenzoic acids. 相似文献
110.
Kazuyuki MiyashitaHidenobu Murafuji Hiroshi IwakiEito Yoshioka Takeshi Imanishi 《Tetrahedron》2003,59(26):4873-4879
As a second-generation pyridoxal model compound for cystathionine β-synthase, we designed a novel model compound having an ionophore function and an imidazole function, application of which to the β-replacement reaction with various thiols smoothly took place to give S-substituted cysteines. Peptides having a serine-O-carbonate residue at the N-terminal position were also converted to the corresponding peptides having an S-substituted cysteine residue under the catalytic conditions of the novel pyridoxal model compound. 相似文献