Nitrogen compounds amine derivatives

The formation of vinylogous amides from primary amines and -dicarbonyl compounds gives rise to hydrolyzable amine derivatives with greatly decreased nucleophilicity of the nitrogen function. Thus these derivatives have found some use as protecting groups in peptide syntheses 617-619). 

Most of the inhibitors in use are organic nitrogen compounds and these have been classified by Bregman as (a) aliphatic fatty acid derivatives, b) imidazolines, (c) quaternaries, (d) rosin derivatives (complex amine mixtures based on abietic acid) all of these will tend to have long-chain hydrocarbons, e.g. CigH, as part of the structure, (e) petroleum sulphonic acid salts of long-chain diamines (preferred to the diamines), (/) other salts of diamines and (g) fatty amides of aliphatic diamines. Actual compounds in use in classes (a) to d) include oleic and naphthenic acid salts of n-tallowpropylenediamine diamines RNH(CH2) NH2 in which R is a carbon chain of 8-22 atoms and x = 2-10 and reaction products of diamines with acids from the partial oxidation of liquid hydrocarbons. Attention has also been drawn to polyethoxylated compounds in which the water solubility can be controlled by the amount of ethylene oxide added to the molecule. 

Amines are ammonia derivatives in which one or more hydrogen atoms have been replaced by an organic radical. Amines are sometimes called nitrogen bases. Basic chemistries include fatty amines (as primary, secondary, tertiary, and polyamines), amine salts, quaternary ammonium compounds, amine oxides, and amides. 

Proteins are also important nitrogen compounds. They constitute much of the cell materials, and are present in every type of organism known. In humans, muscle tissue, skin, and hair is mostly protein, about half of the dry weight of our bodies. From a chemical point of view, proteins are polymers of amino acids, alpha amine derivatives of carboxylic acids. Only about 20 different amino acids are actually found in proteins. It is the large number of variations in the protein chain, using only these... 

Double asymmetric induction operates when the azomethine compound is derived from a chiral a-amino aldehyde and a chiral amine, e.g., the sulfin-imine 144 [70]. In this case, the R configuration at the sulfur of the chiral auxihary, N-tert-butanesulfinamide, matched with the S configuration of the starting a-amino aldehyde, allowing complete stereocontrol to be achieved in the preparation of the diamine derivatives 145 by the addition of trifluo-romethyl anion, which was formed from trifluoromethyltrimethylsilane in the presence of tetramethylammonium fluoride (Scheme 23). The substituents at both nitrogen atoms were easily removed by routine procedures see, for example, the preparation of the free diamine 146. On the other hand, a lower diastereoselectivity (dr 80 20) was observed in one reaction carried out on the imine derived from (it)-aldehyde and (it)-sulfinamide. 

Cationic surfactants produce a positively charged surfactant ion in solution and are mainly quaternary nitrogen compounds such as amines and derivatives and quaternary ammonium salts. Owing to their poor cleaning properties, they are little used as detergents rather their use is a result of their bacteriocidal qualities. Relatively little is known about the mechanisms of biodegradation of these compounds. 

The amines contain nitrogen bonded to 1, 2, or 3 carbon chains. These compounds are derivatives of ammonia, hence the name of the class, as shown in Figure 6-16. 

Metal-Nitrogen Compounds The cobalt catalyzed reaction of primary and secondary amines with carbon monoxide leads to the formation of formamide derivatives. Dimethylamine, for example, gives iV,i T-dimethvlformamide in 60% yield (90, 91). Very likely cobalt-nitrogen compounds are intermediates which undergo a CO insertion and then reduction. The following mechanism has been suggested for the reaction (90). 

Essential oils may comprise volatile compounds of terpenoid or non-terpe-noid origin. All of them are hydrocarbons and their oxygenated derivatives. Some may also contain nitrogen or sulphur derivatives. They may exist in the form of alcohols, acids, esters, epoxides, aldehydes, ketones, amines, sulphides, etc. Monoterpenes, sesquiterpenes and even diterpenes constitute the composition of many essential oils. In addition, phenylpropanoids, fatty acids and their esters, or their decomposition products are also encountered as volatiles [1-16, 21-33, 36-38]. 

The other nitrogen compounds which are nonbasic, and are not extracted from hydrocarbons by dilute acid, have not been investigated in detail, though there are indications that they contain pyrroles. In addition, it is possible that some part of the nitrogen in this material is present in the form of amides, derived from primary or secondary amines and petroleum acids. 

Unlike ethylene glycol, a-hydroxycarboxylic acids, and p-mercaptoethanol, ligands such as ethanolamine, ethylenediamine, amino acids, and 2-aminoethanethiol do not form V2L2 complexes with vanadate [46], However, weakly formed products of VL stoichiometry (—546 ppm, —556 ppm) are observed with a number of a-amino acids [47], Because the amine functionality in amino acids is not suitable for formation of the cyclic [VN]2 core expected for a dimer, then one or the other of these VL compounds may correspond to the monomeric precursor to such a dimeric product. Certainly, with the a-hydroxycarboxylic acids, the monomeric complex can be a major component in solution. Similar VL complexes have not been reported for the amino alcohols. Perusal of the available reports suggests that the amine derivatives were studied under conditions where the nitrogen functionality was protonated, so the results may be somewhat misleading. 

Kinetic results concerning catalytic hydrogenative destruction of heterocyclic nitrogen compounds have been published by Cox and Berg.21 In their operating condition (370°C, 17 atm, space velocity 0.5-20 h 1, which does not affect the rate of HDN, wt% N < 2.5%), they found that most of the five membered ring compounds (pyrrole derivatives and indole) follow a second-order law with respect to the amine pressure, while a first-order law is shown for six membered ring compounds (pyridine and derivatives). 

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