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SUBJECTS precursors

Chromatographic techniques coupled with mass spectrometry (GC-MS, GC-MS/MS, LC-MS and LC-MS/MS) have also been applied in many combinations. A library of reference mass spectra is an integral part of each type of GC-MS apparatus, enabling typing of spectra that are potentially similar to the identified compound. For the GC-MS-EI technique, a combination of two previously separate libraries, Wiley and NIST 2008 (W8/N08), should be mentioned because of its extensiveness. Library W8/N08 contains 562,000 El spectra, 5308 spectra of parent ions (precursors) subjected to fragmentation by the MS/MS technique, over 2 million names of chemical compounds and their synonyms, 35,000 structural formulae and 43,000 GC retention indices. The Automated Mass Spectrometry... [Pg.322]

Finding 3-2. Neutralization of the binary precursors DF and QL is feasible but generates substantial quantities of liquid wastes that contain CWC Schedule 2 precursors subject to oversight and inspection by the Organization for the Prohibition of Chemical Weapons. Posttreatment to destroy these secondary wastes will be required. [Pg.70]

Kobayashi and co-workers introduced 2-(trimethylsilyl)phenyl triflate as an aryne precursor subject to benzyne formation without the need of a strong base. Fluoride-induced desilylation and rapid elimination of the sulfonate provide efficient access to benzyne in acetonitrile at room temperature (eq 1). Other solvents such as THF, acetone, dichloromethane, DME, and toluene may be used, but such conditions may require heating for benzyne formation and frequently afford diminished yields. Preparation of the benzyne intermediate is even possible in protic media, albeit with decreased efficiency and limited applicability in subsequent reaction steps. ... [Pg.639]

Anilines react with ct-haloacetophenones to give 2-arylindoles. In a typical procedure an W-phenacylaniline is heated with a tw o-fold excess of the aniline hydrobromide to 200-250°C[1]. The mechanism of the reaction was the subject of considerable investigation in the 1940s[2]. A crucial aspect of the reaction seems to be the formation of an imine of the acetophenone which can isomerize to an aldimine intermediate. This intermediate apparently undergoes cyclization more rapidly (path bl -> b2) than its precursor (Scheme 7.3). Only with very reactive rings, e.g, 3,5-dimethoxyaniline, has the alternative cydiz-ation (path al a2) to a 3-arylindole been observed and then only under modified reaction conditions[3],... [Pg.77]

Eigure 2 shows that even materials which are rather resistant to oxidation ( 2/ 1 0.1) are consumed to a noticeable degree at high conversions. Also the use of plug-flow or batch reactors can offer a measurable improvement in efficiencies in comparison with back-mixed reactors. Intermediates that cooxidize about as readily as the feed hydrocarbon (eg, ketones with similar stmcture) can be produced in perhaps reasonable efficiencies but, except at very low conversions, are subject to considerable loss through oxidation. They may be suitable coproducts if they are also precursors to more oxidation-resistant desirable materials. Intermediates which oxidize relatively rapidly (/ 2 / i — 3-50 eg, alcohols and aldehydes) are difficult to produce in appreciable amounts, even in batch or plug-flow reactors. Indeed, for = 50, to isolate 90% or more of the intermediate made, the conversion must... [Pg.337]

X-ray diffraction work (11,15) shows that there is an ionomer peak at 4°C which is absent in the acid precursor. This low, broad peak is not affected by annealing or ion type and persists up to 300°C. Since the 4°C peak corresponds to a spacing of about 2.5 nm, it is reasonable to propose a stmctural feature of this dimension in the ionomer. The concept of ionic clusters was initially suggested to explain the large effects on properties of relatively sparse ionic species (1). The exact size of the clusters has been the subject of much debate and has been discussed in a substantial body of Hterature (3,4,18—20). A theoretical treatment has shown that various models can give rise to supramoleculat stmctures containing ionic multiplets which ate about 10 nm in diameter (19). [Pg.407]

The chemistry and stereochemistry of aminoboranes containing the siLicon—nitrogen—boron linkage have been the subject of numerous studies. Many of these compounds are useful precursors to other B—N systems including diboryl-amines (45) and B—H substituted aminoboranes (46). A series of... [Pg.262]

Site-specific deuterium labeling of steroids can also be accomplished by biosynthetic procedures, using deuterated precursors, but these methods are beyond the scope of this chapter. For reviews of this subject see, for example, ref. 45, 54 and 55. [Pg.212]

Electron irradiation (100 keV) of the sample, heated to 800°C, yields MWCNTs (20-100 nm in length) attached to the surface. Such nanotube growth does not take place if natural graphite, carbon nanoparticles or PTFE are subjected to electron irradiation. The result implies that the material may be a unique precursor for CNTs and may constitute a new preparation method. [Pg.150]

Vanhanen, H. X, Blomqvist, S., Ehnholm, C., et al., 1993. Sernm cholesterol, cholesterol precursors, and plant sterols in hypercholesterolemic subjects widi different apoE phenotypes during dietary sitostanol ester treatment. Journal of Lipid Research 34 1535-1544. [Pg.258]

During studies on ditryptophan derivatives, an interesting acid-induced cy-cHzation has been discovered. The 10-membered ring 37 was thus subjected to acidic conditions to produce the indolocarbazole derivative 38 (Scheme 6). Interestingly, calculations performed on the precursor 37 indicated that the lowest energy conformation resembled that of the diastereomer of 38, which was never observed. An additional experiment furnished the parent system 1 on treatment of 38 with a catalytic amount of acid. A TFA-induced formation of an indolo[2,3-<3]carbazole was also observed from a related acyclic 2,2 -connected tryptophan dimer (99JOC8537). [Pg.9]

Before getting to the main subject of this chapter—the reactions of alkenes— let s take a brief look at how alkenes are prepared. The subject is a bit complex, though, so we ll return in Chapter 11 for a more detailed study. For the present, it s enough to realize that alkenes are readily available from simple precursors— usually alcohols in biological systems and either alcohols or alkyl halides in the laboratory. [Pg.214]

Summary term for a number of steroid hormones and their precursors with differentiation-inducing activity in many tissues. As regards bone, three components are relevant cholecalciferol ( vitamin D ) 25-hydroxyvi-taminD3 (calcidiol) and 1,25-dihydroxy vitamin D3 (calcitriol). The latter is the biologically active form and increases both intestinal calcium absoiption and bone resorption. Vitamin D preparations are widely used for the treatment of osteoporosis. Daily supplementation with vitamin D reduces bone loss in postmenopausal women and hip fractures in elderly subjects. [Pg.1294]


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