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151.
The aep-PNA is a chiral and cyclic PNA analogue, which has a stronger and base dependent binding affinity with complementary DNA. To understand the base dependent properties at monomer level, the structural studies of aep-PNA-(T/C/A) monomers have been carried out focussing on the conformational analysis of pyrrolidine ring pucker in aep-PNA by 1H NMR and the coupling constant data fitted into PSEUROT software. The results indicate that the type of pyrrolidine pucker depends on the electronic nature of substituent, implying the effect of pyrimidine or purine substituents in determining the ring pucker in monomers. This may consequently influence the aep-PNA oligomer conformation. Since pyrrolidine nucleic acids have emerged as an important class of PNA analogues, present results may have importance for their future development. 相似文献
152.
Novel camphor sulfonamide based organocatalysts were evaluated for their catalytic activity in the Michael reaction of ketones with nitroolefins. Reaction of ketones with β-nitrostyrenes in the presence of 20 mol % organocatalyst 1a and benzoic acid under solvent-free conditions at 0 °C provided the desired Michael adducts with high chemical yields (up to 97%) and excellent stereoselectivities (>99:1). 相似文献
153.
154.
Bala Karlo Brcanov Dejan Gvozdenović Nebojša 《Central European Journal of Operations Research》2017,25(3):525-543
Central European Journal of Operations Research - In this paper we study a problem that arose while planning the delivery of perishable goods, such as newspapers or foodstuff, in urban areas. The... 相似文献
155.
Kurt M. Bretthauer Bala Shetty Siddhartha Syam 《The Journal of the Operational Research Society》1996,47(3):457-462
In this paper we present a new branch and bound algorithm for solving a class of integer quadratic knapsack problems. A previously published algorithm solves the continuous variable subproblems in the branch and bound tree by performing a binary search over the breakpoints of a piecewise linear equation resulting from the Kuhn-Tucker conditions. Here, we first present modifications to a projection method for solving the continuous subproblems. Then we implement the modified projection method in a branch and bound framework and report computational results indicating that the new branch and bound algorithm is superior to the earlier method. 相似文献
156.
The optical absorption spectrum of Ni2+ ion doped in lecontite (sodium ammonium sulphate dihydrate) single crystal has been studied at room and liquid air temperatures. All the bands could be assigned assumingO h symmetry for the Ni2+ ion in the crystal. The splitting of3 T 1g (F) band at liquid air temperature has been attributed to spin-orbit interaction. The crystal field and spin-orbit parameters derived areD q=1000 cm?1;B=740 cm?1;C/B=4.27 and ζ=600 cm?1. All the bands observed show a blue shift when the crystal was cooled to liquid air temperature. 相似文献
157.
K. R. Krishna Iyer P. Neelakantan T. Radhakrishnan 《Journal of Polymer Science.Polymer Physics》1968,6(10):1747-1758
The Rayleigh-Gans theory of light scattering by a homogeneous cylinder has been applied to the case of scattering by a pad of fibers immersed in a liquid. The theory enables one to locate precisely the matching wavelength at which the mean refractive index of a sample of optically heterogeneous fibers coincides with that of an immersion medium. Thereby it offers a method of determining the mean refractive index. Besides, it facilitates a quantitative estimation of the variability of refractive index. The new technique has been used to study the birefringence of untreated cotton and ramie. The results are presented and discussed. 相似文献
158.
Literature reports have described the covalent coupling of the primary amine-containing anticancer drug, adriamycin, to polymeric supports through the amine group on the drug. These reports also have described drug mechanism studies with the immobilized adriamycin, where the release of the drug would undermine the validity of the conclusions. In the present paper, detailed experimental conditions are given for preparation of nonwater-soluble particles of polyvinyl alcohol by crosslinking water-soluble polyvinyl alcohol with 1,4-benzenedicarboxaldehyde, and for activation with cyanuric chloride and covalent attachment of adriamycin. The expected stability of this drug-support linkage against hydrolytic cleavage is compared mechanistically to that expected for less stable coupling through a carbamate linkage or for less stable coupling via an azomethine link. 相似文献
159.
Kinetics of the acid hydrolysis of acetophenone exime and its substituted compounds have been investigated polarographically. A detailed study of the hydrolysis of acetophenone oxime in 0·05–1·0 M HCl indicated that the rate determining step varied with acid concentration. The reaction in acid concentrations below 0·3M is catalysed by hydrogen ions while general base catalysis by water is predominant in high acid concentrations. Addition of methanol is found to decrease the rate of hydrolysis predominantly. 相似文献
160.
Vanda Veprek-Bilinski Krishna Narasimhan Andr S. Dreiding 《Helvetica chimica acta》1978,61(8):3018-3027
Reaction of Diphenylcyclopropenone with β-Carbonyl-enolates. I. Use of Acetylacetone, Methyl Acetoacetate, 2-Ethoxycarbonyl-cyclododecanone and Dimethyl Malonate The reaction of the sodium salts of acetylacetone ( 6 ), methyl acetoacetate (7) , 2-ethoxycarbonyl-cyclododecanone (8) , dimethyl malonate (19) and its methyl derivative 20 with diphenylcyclopropenone ( 5 ) in dimethylformamide at room temperature led to the unsaturated γ-lactones 14, 15, 17, 22 and 36 . In the case of dimethyl malonate ( 19 ), the halfester 21 , the acyl-malonic ester 24 and the indenone-malonic ester 23 were also isolated. Several intermediates and the final products were characterised by reactions and spectroscopically. A general mechanism is discussed for the addition of cyclo-propenones ( 1 ) to the enolate salts of β-dicarbonyl compounds 4 involving the bicyclic lactone-enolates 18 and 32 as intermediates. The products formed via 18 and 32 are considered to be the result of an attack of one of the oxygen atoms of the β-carbonyl-enolate anion ( 4 ), the product 24 , on the other hand, of the attack of the α-carbon atom of 4 ; in both cases the attack is on the carbonyl C-atom of 5 . 相似文献