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Special Compounds

The cyclic diazo compounds (diazirines 65) are very unreactive compounds. Specially noticeable is the absence of the reactivity toward electrophilic reagents which is characteristic of the linear isomers. Acids or aldehydes which react smoothly with the aliphatic diazo compounds are without action on the cyclic diazo compounds. Iodine does not attack the cyclic diazo compounds. [Pg.126]

Pharmacists are also responsible for compounding special ear preparations for pets that are not commercially available. Sometimes the availability and cost of certain medications are prohibitive for a veterinarian s private pharmacy. [Pg.728]

Fire and Explosion Hazards of Peroxy Compounds, Special Publication No. 394, Castrantas, H. M., Banerjee, D. K.,... [Pg.1928]

Sturmer DM (1977) Syntheses and properties of cyanine and related dyes. In Weissberger A, Taylor EC (eds) The chemistry of heterocyclic compounds special topics in heterocyclic chemistry. Wiley, New York... [Pg.185]

Studies of the effects of low frequency ultrasonic waves on a broad range of synthetically useful reactions are summarized. Discussion is centered on the results obtained in our laboratory where we have concentrated on the reactions of metals with functionalized organic and organometallic compounds. Special emphasis is on lithium and zinc with organic and organosilicon halides. [Pg.213]

Abstract. This article describes recent achievements of my research group in the Leibniz-Institut fiir Katalyse e.V. in the area of applied homogeneous catalysis for the synthesis of biologically active compounds. Special focus is given on the development of novel and practical palladium and copper catalysts for the functionalization of haloarenes and haloheteroarenes. [Pg.99]

In the first part of this review a critical analysis of various criteria of aromaticity and the indices quantifying aromatic or antiaromatic character is presented in Section II with an emphasis on application to heterocyclic compounds. Special attention is paid to the elucidation of general trends observed in the change of aromatic character on going from the parent... [Pg.305]

In this chapter, preparation and purification methods are reviewed. In view of the expected role of 5 f electrons in the metallic bond of actinides, methods for the preparation of metals have been particularly studied. There has also been important progress in the preparation of simple binary compounds. Special emphasis has been given to the growth of single crystals, particularly needed for the most refined physical techniques. [Pg.57]

For seven other space groups, rarely found with organic compounds, special coordinate transformations are necessary39,40. [Pg.386]

Therefore, the reaction of an epoxy compound with amine can proceed in the absence of hydroxyl-containing compounds specially added or occurring as impurity, the amine acting both as a nucleophilic and an electrophilic reagent. [Pg.118]

First let us consider the initiation process in the presence of proton-donor compounds specially introduced into the system. Two contradictory viewpoints about the reaction mechanism may be distinguished in this case. One of them 138,139f l45,154) presupposes a molecular mechanism of the reaction, i.e. a stepwise polyaddition of the epoxy compound to the alcohol group, e.g. according to Scheme (32)... [Pg.150]

Electrolytic processes for the perchlorates.—F. von Stadion found that if an aq. soln. of chlorine dioxide be included in Volta s circuit, at first very little gas is developed, but after some hours, oxygen and chlorine appear at the anode, and hydrogen at the cathode. The volume of hydrogen so obtained is nearly twice that of the oxygen. After some time the soln. is decolorized, and transformed into perchloric acid. In 1857, A. Riche 18 prepared perchloric acid by the electrolysis of hydrochloric acid, or of an aq. soln. of chlorine and ten years earlier, H. Kolbe prepared potassium perchlorate by the electrolysis of an aq. soln. of potassium chloride—acidified with sulphuric acid—and of potassium trichloro-methyl-sulphonate. H. Kolbe (1846), a pioneer in the electrolytic preparation of compounds, specially noted that the formation of perchloric acid is always preceded by that of chloric acid, and stated ... [Pg.374]

If Aisc > (Aic + A/ ) as is generally the case for many organic compounds, specially heteroaromatic hydrocarbons, the intrinsic phosphorescence efficiency is given by... [Pg.152]

Castrantas, H.M. and Banerjee, D.K., Laboratory Handling and Storage ofPeroxy Compounds, Special Publication No. 491, American Society for Testing and Materials, Philadelphia, 1970. [Pg.442]

Coincident with the development of sampling procedures were the constant iterative improvements in extraction, separation, identification and quantitation of organic compounds. Special emphasis was placed on selected compound classes such as the polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), chlorinated benzenes, and chlorinated dibenzo-p-dioxins (dioxins). The best available procedures were used to determine these components because they have known acute or chronic effects and previous studies suggested that they might be present in effluents from the combustion of coal alone and combination coal/RDF. [Pg.116]

Field desorption M+ Mg-ng Non volatile compounds Specialized equipment... [Pg.8]


See other pages where Special Compounds is mentioned: [Pg.351]    [Pg.202]    [Pg.1147]    [Pg.11]    [Pg.95]    [Pg.500]    [Pg.48]    [Pg.297]    [Pg.1255]    [Pg.268]    [Pg.463]    [Pg.341]    [Pg.359]    [Pg.169]    [Pg.281]    [Pg.282]    [Pg.283]    [Pg.80]    [Pg.83]    [Pg.84]    [Pg.21]    [Pg.308]   


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Compounding and Special Additives

Compounding ingredients, special

Compounding ingredients, special plasticizers

Compounding ingredients, special resins

Compounding special design

Compounds, special classes

Compounds, special classes steroids

Compounds, types of reactions, special apparatus, and unfamiliar methods

Fabricating products specialized compounding

Organometallic compounds special techniques

Rubber Compounds with Special Mechanical Properties

Special Groups of Heterocyclic Compounds

Special Topic 6.18 Photoactivatable compounds

Special Topic 6.6 Photochemical synthesis of cage compounds

Speciality compounds

Speciality compounds

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