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Nuclear Modifications

It has been found empirically that central analgesics that possess some degree of activity as antagonists of the effects of morphine tend to show a reduced propensity for causing physical addiction. Again empirically, it was noted that this could often be achieved by replacement of the N-methyl group by allyl, cyclopropylmethyl, or cyclobutylmethyl additional nuclear modifications often contributed to this activity. [Pg.111]

A subsidiary approach involves nuclear modification of the arylsilanes so obtained. The requisite organometallics can be prepared from aryl halides, or by deprotonation of a suitably activated (c.g. methoxy-substituted) arene. A more specialized route involves cycloaddition between alkynylsilanes and diynes. [Pg.114]

Most common among the nuclear modifications is the saturation and desaturation that results in the many olefinic isomers, some of which are exceedingly rare... [Pg.16]

The discovery of the /8-lactamase inhibitory activity of sulbactam signalled a resurgence of interest in the nuclear modification of 6-APA (8). Micetich and co-workers concentrated their efforts on the synthesis of 2-/8-... [Pg.329]

Nuclear modification of imidazoles continue to be popular research topics. Seouential metallation of the phenylimidazole (55) afforded the trisubstituted imidazole (56) [94TL(35)3817]. Subtle reactivity differences were observed when 2-lithioimidazole (57a, W = trityl, R = = H) was quenched with f-butyl haloacetates. lodination and... [Pg.152]

An alternative to both the limited or nuclear modification of natural substances is total synthesis. In addition to comments on the results of total synthesis included in the Dedication, Volume 2 has two chapters (2 and 5) devoted to a description of the technology and the compounds obtained by this route. The diversity of p-lactam-containing structures retaining antibacterial activity lends credence to the postulation by Strominger and Tipper in 1965 of implied minimal structural requirements for biological activity. [Pg.611]

During many years in Scientific Research Institutes of Nuclear Physics and Introscopy at Tomsk Polytechnical University (TPU) researches into induction electron accelerators and their uses for non-destructive radiation quality control of materials and articles have been conducted. Control sensitivity and efficiency detection experimental researches have been conducted with the high-current stereo-betatron modifications [1], and KBC-25 M and BC-50 high-current betatrons [2,3] in range of 11 MeV and 25-50 MeV radiation energy. [Pg.513]

Cordonnier M, Uy D, Dickson R M, Kew K E, Zhang Y and Oka T 2000 Selection rules for nuclear spin modifications in ion-neutral reactions involving Hg" J. Chem. Phys. 113 3181-93... [Pg.1092]

The success of the Bart reaction when applied to nuclear- substituted anilines is often much affected by the pH of the reaction-mixture. Furthermore, the yields obtained from some m-substituted anilines, which under the normal conditions are usually low, arc considerably increased by the modifications introduced by Scheller, and by Doak, in which the diazotisation is carried out in ethanolic solution followed by reaction with arsenic trichloride in the presence of a cuprous chloride or bromide catalyst. [Pg.312]

Replacing the nuclear and electronic momenta by the modifications shown above in the kinetic energy terms of the full electronic and nuclear-motion hamiltonian results in the following additional factors appearing in H ... [Pg.377]

The recycle weapons fuel cycle rehes on the reservoir of SWUs and yellow cake equivalents represented by the fissile materials in decommissioned nuclear weapons. This variation impacts the prereactor portion of the fuel cycle. The post-reactor portion can be either classical or throwaway. Because the avadabihty of weapons-grade fissile material for use as an energy source is a relatively recent phenomenon, it has not been fully implemented. As of early 1995 the United States had purchased highly enriched uranium from Russia, and France had initiated a modification and expansion of the breeder program to use plutonium as the primary fuel (3). AH U.S. reactor manufacturers were working on designs to use weapons-grade plutonium as fuel. [Pg.202]

Giaphite with its exceptional strength and thermal stabiUty at high temperatures is a prime candidate material for many aerospace and nuclear appHcations. Its properties, through process modifications, are tailorable to meet an array of design criteria for survival under extremely harsh environmental operations. [Pg.513]

NRA as in RBS or ERDA, and possible modification of the target composition as a result of irradiation must be considered. Nuclear reaction cross-sections are also usually not available in analytical form for direct evaluation of measured data. Concentrations are, therefore, often obtained by comparison of the measured data with results from standard samples of known concentration. [Pg.171]

The molecular and bulk properties of the halogens, as distinct from their atomic and nuclear properties, were summarized in Table 17.4 and have to some extent already been briefly discussed. The high volatility and relatively low enthalpy of vaporization reflect the diatomic molecular structure of these elements. In the solid state the molecules align to give a layer lattice p2 has two modifications (a low-temperature, a-form and a higher-temperature, yS-form) neither of which resembles the orthorhombic layer lattice of the isostructural CI2, Br2 and I2. The layer lattice is illustrated below for I2 the I-I distance of 271.5 pm is appreciably longer than in gaseous I2 (266.6 pm) and the closest interatomic approach between the molecules is 350 pm within the layer and 427 pm between layers (cf the van der Waals radius of 215 pm). These values are... [Pg.803]

An X-ray crystallographic study of 2-hydroxy-4,6-dimethylpyrimi-dine led to no conclusions regarding its structure. Because of the rapid exchange of the NH protons of pyrimidin-2-one both in dimethyl sulfoxide and in water, nuclear magnetic resonance spectroscopy does not afford positive evidence for either the oxo or the hydroxy formulation. The statement that 4,6-dimethylpyrimidin-2-one had been isolated in two modifications, 94 and 95, was soon disproved. ... [Pg.370]

Bloom M., Bridges F., Hardy W. N. Nuclear spin relaxation in gaseous methane and its deuterated modifications, Can. J. Phys. 45, 3533-54 (1967). [Pg.279]


See other pages where Nuclear Modifications is mentioned: [Pg.16]    [Pg.17]    [Pg.1160]    [Pg.205]    [Pg.476]    [Pg.16]    [Pg.17]    [Pg.1160]    [Pg.205]    [Pg.476]    [Pg.1828]    [Pg.2092]    [Pg.9]    [Pg.203]    [Pg.7]    [Pg.202]    [Pg.324]    [Pg.324]    [Pg.325]    [Pg.81]    [Pg.163]    [Pg.37]    [Pg.180]    [Pg.711]    [Pg.276]    [Pg.765]    [Pg.369]    [Pg.495]    [Pg.978]    [Pg.1026]    [Pg.1166]    [Pg.1166]    [Pg.1166]    [Pg.1167]    [Pg.1265]    [Pg.464]   


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