Two new partially saturated tricyclic ring systems, , a, 7, , , 10, 10a, 11-octahydro-11-oxodibenz [, ] oxepins (3a and 3), and -thiepins (a and ) were synthesized. Compounds a and were desulfurized to give a pair of isomeric 2-methylbenzoylcyclohexanes (10a and 10). Deuterated a and (11a and 11) were prepared starting from butadiene- (12). The stereochemical features of 3a (trans), 3 (cis), a (trans) and (cis) are compared with those of 10a, 10, 11a and 11 on the basis of proton nuclear magnetic resonance data.

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The phase diagrams of the Ni-Mo- and Ni-W- ternary systems in the region of less than 50mol% were constructed by thermodynamic calculation, based on the data obtained by thermodynamic measurement of the related materials. We found three ternary eutectic points and three or two ternary peritecto-eutectic points as follows:
:L (1365K, 71.mol%Ni-.mol%Mo-.mol%)=(Ni)++
:L (1355K, 62.mol%Ni-2.mol%Mo-30.mol%)=++
:L (1445K, 42.mol%Ni-30.mol%Mo-10.3mol%)=(Ni)+NiMo+
P₁:L (1812K, 34.mol%Ni-42.3mol%Mo-.mol%)+MoB=+
P₂:L (1633K, 42.3mol%Ni-40.mol%Mo-17.3mol%)+Mo=+
P₃:L (1812K, 53.mol%Ni-33.7mol%Mo-12.mol%)+Mo=NiMo+
:L (1622K, 51.mol%Ni-31.mol%W-17.mol%)=(Ni)+W+
:L (1260K, 71.mol%Ni-7.mol%W-.mol%)=(Ni)++
:L (1291K, 65.mol%Ni-.mol%W-29.mol%)=++
P₁:L (2115K, 23.mol%Ni-43.1mol%W-33.1mol%)+WB=+
P₂:L (1657K, 48.mol%Ni-33.1mol%W-18.mol%)+=W+
The calculated phase diagrams are expected to be useful for the development of new Ni-based heat-, corrosion- or wear-resistance alloys.

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11-Amino-, a, 7, , , 10, 10a, 11-octahydrodibebenzo[, ]thiepines (a-d) and -oxepines (7a-d) were synthesized by the Leuckart reaction of , a, 7, , , 10, 10a, 11-octahydro-11-oxodibenzo[, ]thiepines (1a, )and -oxepines (2a, ) followed by hydrolysis of the reaction products a-d and a-d, respectively. The four diastereomers, cis(a-H, 10a-H)-cis(10a-H, 11-H) a and 7a, cis(a-H, 10a-H)-trans(10a-H, 11-H) and 7, trans(a-H, 10a-H)-trans(10a-H, 11a-H)c and 7c, and trans(a-H, 10a-H)-cis(10a-H, 11-H) d and 7d, were isolated and their configurations and conformations were elucidated by chemical methods together with ¹H-nuclear magnetic resonance spectroscopic and X-ray crystallographic analyses.

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This study aimed to determine the prevalence of fecal carriage of extended spectrum β-lactamase (ESBL) and/or plasmidic AmpC β-lactamase (pAmpC) producing Escherichia coli among dogs (n=428) in Turkey. Polymerase chain reaction (PCR) and sequencing were used to characterize genes encoding β-lactamase and plasmid mediated quinolone resistance (PMQR). Antimicrobial susceptibility testing and PCRs for virulence genes and phylogenetic groups were also performed. Cefotaxime resistant

. coli isolates were detected in 95 (.2%) of the swab samples. Sequencing analysis results showed occurrence of various β-lactamase genes: bla_CTX-M-15 (62), blaTEM-

1b

(42), bla_CMY-2 (

22

), bla_CTX-M-3 (16), bla_CTX-M-1 (15), bla_OXA-1 (

9

) and bla_SHV-12 (3) alone or in combination. The most frequently encountered phylogenetic group was group A₁ (35.

8

%), followed by group D₂ (

22

.1%),

B

1 (15.

8

%), D₁ (

9

.

5

%),

A₀

(7.

4

%),

B2₂

(

5

.3%) and

B2₃

(

4

.2%), respectively. PMQR genes, aac(

6

’)-Ib-cr, qnrS1 and qnrB10 were detected in 25.3, 10.

5

and 1.1% of the isolates, respectively. While all isolates were susceptible to imipenem and amikacin, resistance rates to non-β-lactam antibiotics ranged from 20.

0

% for tobramycin to 56.

8

% for tetracycline. The virulence genes were only detected in 34 (36.2%) of the isolates and this isolates carried single or various combination of virulence genes of iucD, papC, papE, f17a-A and eaeA. Four isolates were identified as human virulent pandemic CTX-M-15 producing

E

. coli clone O25

b

:ST131/

B

2. To the best of our knowledge, this is the first study to show fecal carriage of ESBL/pAmpC type β-lactamase producing

E

. coli isolates among dogs in Turkey.

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We compared three groups of pregnant women: placebo with normotensive women, group A which included preeclamptics, and group which comprised preeclamptics who were supplemented their diets with vitamins C and . MDA increased from . ± 2. (placebo) to .48 ± 1.2 (A) and .02 ± 1. nmol/gHb (). NO concentrations were enhanced from 19.3 ± .2 (P) to 23. ± . (A) and 24.1 ± . μmol/L (). GSH contents were decreased from 10.42 ± 2.81 (P) to .02 ± 2.92 (A) and .39 ± 1.02 μmol/g Hb (), whereas GSSG concentrations increased from .98 ± .28 (P) to 1.24 ± .29 (A) and 1.08 ± .12 μmol/g Hb (). SOD activity decreased 23% in A and 14% in ; GRx decreased 27% in A and .% in ; GPx decreased 12% in A and .% in . Catalase activity, however, increased 27% in A and 29% in as compared to control. Thus, we conclude that the use of vitamins C and should be considered for the control of certain important biochemical indices during the development of preeclampsia; however, further studies are needed to develop methods for the prevention of preeclampsia in women at high risk.

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One method currently being considered for the disposal of high level radio-active waste is burial in the seabed. When a hot object is buried in soil, the temperature of the soil adjacent to the object is raised and there is transient heat flow away from the object. The rise in the temperature of the soil causes excess pore pressures to be generated and transient pore water diffusion also takes place. A finite element formulation of the coupled heat flow and consolidation problem is presented. The computer implementation of this formulation is found to compare favourably with analytical solutions based on the same physical principles.

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Stereoselective synthesis of the , -syn, , -anti adducts (14 and 16) on the aldol condensation of the Z (O)-lithium enolate, derived from the -enone (2), to α-alkoxy aldehydes (12 and 13) was proved via the successive intramolecular Diels-Alder reaction.

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This paper outlines a mathematical description of the stress dilatancy behaviour of granular materials which accounts for stress level and void ratio dependencies. The consideration of these aspects has important implications in the modelling of granular material behaviour. In fact, granular material mechanical response is largely dominated by the evolution of dilatancy, fabric and void ratio histories. The starting point in this study is the well established Rowe's theory which is revisited and ultimately modified by introducing a factor linked to governing state parameters in order to describe the complete behaviour of granular materials during deformation. Numerical simulations of triaxial tests on granular materials at different void ratios and stress levels are herein presented to illustrate the model.

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Melithasterols A-D (1-), isolated from a gorgoinan coral Melithaea ocracea of Okinawa, were shown to be cholestane-, 24-methyl--dehydrocholestane-, -dehydrocholestane-, and 24-methylenecholestane-derivatives. respectively, having a common 3β, 7α -dihydroxy-α, α-epoxy-Δ^ steroid nucleus. This was confirmed by direct comparison with the authentic sample prepared by lead tetra-acetate oxydation of cholest--ene- 3β, α, α-triol 3-monoacetate. Twelve new polyhydroxysterols were isolated from an Alcyonium sp. (7,,), and Sclerophytum sp. (14,16,19,20,21,a,23,26,28) soft corals collected off the coasts of the Andaman and Nicobar Islands in the Indian Ocean. All the Sclerophytum sp. soft corals contained 17a or its 25-deacetyl derivative. Compounds 7 to were identified as 24-methylenecholest--ene- 3β, 16β-diol-3--α-L fucoside (7) and its 7β-() and 7α-hydroxy () derivatives. Compound 14 was shown to be 24S-24-methylcholest--ene-3β,25ξ,26-triol and was correlated to the known compound 15 by α, β-glycolation. Compound 16 was shown to be β, α-isomer of 17, correlating to 17 by PCC oxidation followed by dehydration. Compound 19 was identified with 25-deacetyl derivative of the known compound lobosterol (19a) by hydrolysis of authentic lobosterol. Compounds 20 and 21 were shown to be 7-dehydro-(20) and -dehydro-(21) derivative of 17a and 17, respectively, by comparisons of their spectral data with reference compounds. Compounds a and 23 were 24S-methylcholestane-3β, α 25-triol--one 25-monoacetate (a) and its 25-deacetoxyl derivative (23). Partial PCC oxidation of 17a afforded a. Compounds 26 (andamansterol) and 28 (nicobarsterol) were shown to be gorgost--ene-3β, α. 11α, 21-tetrol and novel secosteroid, 11,21-cyclo--homo-11-oxa-, 11-secoergostane-3β, α, 12ξ-triol--one, respectively, by spectral analyses (H-HCOSY, HMQC, HMBC).

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The possibility of attenuation of microseismic waves due to the presence of an upward folding of the ocean bottom into the liquid is discussed in this paper. The upward folding of the ocean bottom has been idealized by means of an irregularity in the form of a rectangle intruding into the liquid and the evaluation of the displacement component at any point of the solid medium has been carried out in two stages. First, the change in the incident mode of the surface wave due to the presence of the rectangular irregularity has been determined, and second, the subsequent change of the resulting displacement components due to the termination of the liquid layer and the step change in elevation of the solid medium at the continental margin has been discovered. Finally, numerical calculation has been made to determine the attenuation of the microseismic waves of different periods due to the presence of the rectangular irregularity at the ocean bottom.

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Brassinolide analogues, (R, 23R, 24R)-2α, 3α, , 23-tetrahydroxy--homo-7-oxa--ergostan--one (24-epibrassinolide) (10) and (S, 23S, 24R)-2α, 3α, , 23-tetrahydroxy--homo-7-oxa--ergostan--one (), were synthesized from brassicasterol (3a) in five steps and with ca. 20% overall yield. The key steps are the direct formation of (, 24R)-3α, -cyclo--ergost--en--one () from brassicasterol mesylate (3), the acid-catalyzed rearrangement of to (, 24R)--ergosta-2, -dien--one (), and the Baeyer-Villiger oxidation of the tetrahydroxy -ergostan--ones 7 and .

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As a fundamental study on dibenzothiepins, reaction of 11-phenyl-, 11-dihydrodibenzo [, ] thiepin-11-ol (10) or 11-chloro-11-phenyl-, 11-dihydrodibenzo [, ] thiepin (14) with triphenylmethyl cation or was examined under various conditions. 11-Phenyl-, 11-dihydrodibenzo [, ] thiepin-11-ylium salt () was isolated as a black powder (perchlorate) and a green powder (hexachloroantimonate), but salt was obtained only as a solution. Treatment of the hexachloroantimonate with excess of was found to result in a novel dehydrocyclization reaction to give selectively , 13-dihydrofluoreno [1, a, -c, d] [2]-benzothiepin-13-ylium hexachloroantimonate (19). Some discussions were made on the mechanism of the formation of 19.

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Plasma concentrations of apolipoproteins (apo) A-I, A-II, , C-II and were measured in the 79 noninsulin-dependent (type II) diabetics. The diabetics consisted of 24 patients on dietary treatment alone (diet group), 16 patients treated with oral hypoglycemic agents (mostly glibenclamide: oral drug group), 15 patients treated with insulin (insulin group) and 24 untreated patients (pretreatment group). The data were analyzed after subdividing each group into the following two subgroup on the basis of fasting blood glucose levels and HbA₁ levels: (1) the patients in good control and (2) the patients in poor control. Mean (±SE) ages were 61.2±2., 59.±2., 61.±2.7, 67.3±.3, 67.±3.7, 58.3±3.2, 59.3±1.7 in diet-good control group, diet-poor control group, oral druggood control group, oral drug-poor control group, insulin-good control group, insulin-poor control group and pretreatment group, respectively. Fasting blood glucose levels and HbA₁ levels in parenthesis were 105.2±2.mg/100ml (7.±.3%), 151.±11.3 (.±.2), .±.2 (.3±.), 162.±13. (11.±.2), 107.7±.3 (.±.), 198.3±16. (11.3±.) and 175.±12. (10.±.) in the groups in the same order as above, respectively. HDL was fractionated by the method of heparin-MnCl₂ precipitation. Plasma apo A-I, A-II, , C-II and were measured by single radial immunodiffusion using the commercially available plate (Daiichi Chemical Pharmaceutical Co., Tokyo). Both plasma cholesterol and triglyceride were significantly higher in the diabetic groups than control. HDL-cholesterol was significantly lower in diet-good control group than control. Plasma apo concentrations were significantly increased in the diabetics (diet-poor control group: 130.±21.mg/100ml, oral drug-good control group: 108.±21.1, insulin-poor control group: 130.±23., pretreatment group: 122.3±23.vs. control group: 87.±20.). Plasma apo C-II concentrations were significantly higher in the diabetics (diet-poor control group: .±2.mg/100ml, insulin-poor control group: .7±1., pretreatment group: .±2.2vs. control group: 2.±.). Plasma apo concentrations were significantly higher in the diabetics (diet-poor control group: .3±2.1mg/ml, insulin-poor control group: .±1., pretreatment group: .±1.3vs. control group: 3.±.). Plasma apo A-I concentrations in diabetics were not significantly different from those of control. Plasma apo A-II concentration was significantly lower in diet-good control group (25.±.3mg/100ml) than control (29.±3.). The effects of diabetic control on plasma apolipoproteins level were investigated. In diet group, plasma concentrations of apo and apo were significantly higher in the diabetics with poor control than those with good control (p<.005 in apo and p<.05 in apo ). In insulin group, plasma concentrations of apo C-II and apo were significantly higher in poor control subgroup as compared to good control subgroup (p<.005 in apo C-II and p<.05 in apo ). In addition, apolipoprotein levels were measured before and after treatment in diabetics. Plasma concentrations of apo , C-II and showed a tendency to decrease with diabetic control. The present study suggested that plasma apolipoprotein concentrations could be one of the indices of metabolic derangement in the noninsulindependent diabetics.

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The solubility and supersolubility of L-phenylalanine in aqueous solutions is firstly reported in this work. At temperatures from 273.15 to 343.15 K, both solubility and supersolubility in water generally increase with the temperature, and the average metastable zone width is about .3°C. At the temperature of 298.15 K, the solubility remarkably decreases with an increase in the concentration of ethanol, which indicates that ethanol can be used as an antisolvent for the precipitation and crystallization of L-phenylalanine. When sodium chloride is added to the solution, the solubility of L-phenylalanine increases with the concentration of sodium chloride.

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Repetitive liquefactions in angular and subangular gravels from an alluvial fan, in the case of two earthquakes with accelerations lower than that of a former which had caused liquefaction some months before, are described. The liquefaction took place from the surface, down to a depth of approximately 10 m. Water laden with sediments spouted out for some tens of minutes after the strong motion ceased. Knowledge of the grain size distribution of the sediments inside the body of the alluvial fan roughly defines the areas of the fan prone to future liquefaction. Non-repetitive liquefaction in overconsolidated fine fluvio-lacustrine sand of glacial origin at the unusual depth of 14 m to 16 m is also described. From the observation of sand lifted up for 10 m inside a large diameter well, and of that which spouted out from several microvents, it was estimated that extra-pore pressure was close to lithostatic conditions. Nevertheless, modeling of intrinsic pore pressure buildup on the DESRA2 programme gives lower values than the experimental one. Geotechnical characteristics of the 12 m-thick sandy stratum indicate that the upper part is unusually soft, either due to water circulation or past repetitive liquefactions which prevented reconsolidation. It is suggested that excess pore pressure generated by the earthquake was also due to redistribution of pressure from adjacent sediments.

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Dialkyl -aryl-2, -dimethyl-1, -dihydropyridine-3, -dicarboxylates (I) were subjected to the Mannich reaction with excess paraformaldehyde and primary amine in ethanolic solution. Novel ring-system compounds, dialkyl t--aryl-1H, H-2, 3, a, 7, , -hexahydro-2, 3a, -triazaphenalene-, γ-a-dicarboxylate derivatives (III), and some intermediary products were obtained stereoselectively. The reaction pathway and the stereochemistry of these products are discussed.

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