Amines dicarboxylic acid reaction with

A new NAD -dependent opine dehydrogenase was purified to homogeneity from Arthrobacter sp. strain 1C isolated from soil by an enrichment culture technique with a synthetic substrate N-[1-DL-(carboxyl)ethyl]-L-phenylalanine [15]. We purified and characterized an NAD+-dependent secondary amine dicarboxylic acid dehydrogenase, and named it opine dehydrogenase (ODH). The enzyme catalyzed a reversible oxidation-reduction reaction of opine-type secondary amine dicarboxylic acids (Scheme 1). 

The first, and still widely used, polymer-supported ester is formed from an amino acid and a chloromethylated copolymer of styrene-divinylbenzene. Originally it was cleaved by basic hydrolysis (2 N NaOH, FtOH, 25°, 1 h). Subsequently, it has been cleaved by hydrogenolysis (H2/Pd-C, DMF, 40°, 60 psi, 24 h, 71% yield), and by HF, which concurrently removes many amine protective groups. Monoesterification of a symmetrical dicarboxylic acid chloride can be effected by reaction with a hydroxymethyl copolymer of styrene-divinylbenzene to give an ester a mono salt of a diacid was converted into a dibenzyl polymer. ... 

In the single-stage production of polyurethanes, di-, tri-, or polyisocyanates are mixed directly with molecules containing two or more reactive hydrogen atoms, such as diols, diamines, and dicarboxylic acids. We typically increase the reaction rate by adding amine or organotin based catalysts. The reaction normally occurs rapidly, evolving much heat. In order to ensure... 

Electrophilic substitution of the ring hydrogen atom in 1,3,4-oxadiazoles is uncommon. In contrast, several reactions of electrophiles with C-linked substituents of 1,3,4-oxadiazole have been reported. 2,5-Diaryl-l,3,4-oxadiazoles are bromi-nated and nitrated on aryl substituents. Oxidation of 2,5-ditolyl-l,3,4-oxadiazole afforded the corresponding dialdehydes or dicarboxylic acids. 2-Methyl-5-phenyl-l,3,4-oxadiazole treated with butyllithium and then with isoamyl nitrite yielded the oxime of 5-phenyl-l,3,4-oxadiazol-2-carbaldehyde. 2-Chloromethyl-5-phenyl-l,3,4-oxadiazole under the action of sulfur and methyl iodide followed by amines affords the respective thioamides. 2-Chloromethyl-5-methyl-l,3,4-oxadia-zole and triethyl phosphite gave a product, which underwent a Wittig reation with aromatic aldehydes to form alkenes. Alkyl l,3,4-oxadiazole-2-carboxylates undergo typical reactions with ammonia, amines, and hydrazines to afford amides or hydrazides. It has been shown that 5-amino-l,3,4-oxadiazole-2-carboxylic acids and their esters decarboxylate. 

Very little work has been done on fluoro derivatives of thiophenes. 2-Fluorothiophene was obtained in low yield from treatment of 2-iodothiophene with arsenic trifluoride. The action of fluoroboric acid on thiophenediazonium salts was unsuccessful. It may be useful for the preparation of 4-, 5-, 6- or 7-fluorobenzo[6]thiophenes from the appropriate amines. However, these are more conveniently prepared from fluorine-substituted benzenethiols by ring-closure reactions. For example 4,5,6,7-tetrafluorobenzo[6 Jthiophene was obtained by decarboxylation of the corresponding 2,3-dicarboxylic acid (equation 99) prepared by condensation of pentafluorobenzenethiol with diethyl acetylenedicarboxylate (Section 3.15.3.4.1). 2-Fluorothiophene has been prepared from 2-thienyllithium using perchloryl fluoride, and 2-fluorobenzo[ Jthiophene from the 2-lithio derivative in a similar manner (Section 3.14.3.9.1). 

Dicarboxylic acids form monomeric complexes with palladium(II), K2[Pd(X2)2] (X2 = oxalate, malonate, etc,).153154 They may be prepared by warming a suspension of palladium(II) chloride with a concentrated solution of the alkali metal dicarboxylate or by using other palladium complexes containing readily substituted ligands such as [Pd(OH)2], [Pd(N03)2(H20)2] or [Pd(02CMe)2]3-155 These complexes are claimed to have useful antitumour properties.155 Complexes [Pd(X2)L2] (X2 = dicarboxylate L = amine or L2 = diamine) may be prepared by reaction of the dichloro complex with a carboxylate salt.156,128... 

Copolymers. There are two forms of copolymers, block and random. A nylon block copolymer can be made by combining two or more homopolymers in the melt, by reaction of a preformed polymer with diacid or diamine monomer by reaction of a complex molecule, eg, a bisoxazolone, with a diamine to produce a wide range of multiple amide sequences along the chain and by reaction of a diisocyanate and a dicarboxylic acid (193). In all routes, the composition of the melt is a function of temperature and more so of time. Two homopolyamides in a moisture-equilibrated molten state undeigo amide interchange where amine ends react with the amide groups. 

Reaction XXXm. (b) Condensation of Malonic Adds with Aldehydes or some Ketones under the influence of Primary or Secondary Amines. (B., 35,1143.)—This is an example of the activating effect of two 1 3 oxy groups on a methylene group between them. In the presence of primary or secondary amines—e.g., ethylamine, di-ethylamine, piperidine— malonic acid condenses with aldehydes and some ketones to give unsaturated dicarboxylic acids. It is probable that the amine reacts first with the aldehyde, water being eliminated. 

Antagonists of metabotropic glutamate receptors and G-protein-coupled receptors associated with various neurodegenerate diseases have been prepared by proline-catalyzed direct a-amination reactions (Scheme 2.30) [7c]. Both, indane carbaldehyde 10 and analogous compounds having an ester functionality [leading to l-aminoindan-l,5-dicarboxylic acid (AIDA)] and or a phosphonate substituent [(RS)-l-amino-5-phosphonoindan-l-carboxylic acid APICA], all reacted with di-... 

As a preliminary step in the manufacture of unsaturated polyester thermoset plastic one uses low molecular weight linear polyester (Mr 10,000) obtained by a polycondensation of polyglycols with saturated and unsaturated dicarboxylic acids. The precondensate can then be dissolved and stored in the stabilized comonomer, e.g. styrene, with which it will be crosslinked later. The crosslinking polymerization reaction between the polyester chains and the styrene bridges is initiated with the help of organic peroxides which are added dispersed in plasticizers. The reaction begins at 60-90 °C and then proceeds exothermally. In addition to this a cold hardening reaction can also be carried out. For this reaction cold accelerators are necessary, e.g. tertiary amines or cobalt naphthenate. 

Cyclizative condensations based on aldol-type reactions which conform to the IIbd pattern have also been developed. Condensation of bis(alkoxycarbonylmethyl)amines or bis(cyanomethyl)amines with benzil affords 3,4-diarylpyrrole-2,5-dicarboxylic acid esters or nitriles. These reactions frequently lead to partial hydrolysis of at least one of the alkoxycarbonyl substituents and if the 3,4-diarylpyrrole is the ultimate objective, work-up involving complete hydrolytic decarboxylation is appropriate (equation 119) (61LA(639)102, 65JOC859). 

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