Aromatization decarboxylation, oxidative

Penicillic acid (Figure 3.45), another micro-bially produced food contaminant with carcinogenic properties, is synthesized by cultures of Penicillium cyclopium and P. baarnense, and also features oxidative ring fission of an aromatic compound. This time orsellinic acid (Figure 3.25) is a precursor, and ring fission appears to proceed via a quinone, which is the result of decarboxylation, oxidation, and methylation reactions. Figure 3.45 also represents an over-simplistic rationalization of the ring fission process. 

Oxidation of amines to ketones, 78-79 Oxidation of hydrazones, 170 Oxidative aromatization, 192 Oxidative condensation, 192 Oxidative coupling, 79, 331-332 Oxidative decarboxylation, 168—169, 238— 239... 

There is a general agreement that the natural phenethylamines are biogenetically linked to the naturally occurring aromatic amino acids, such as phenylalanine, tyrosine, iV-methyltyrosine and 3 4 dihydroxy-phenylalanine (dopa). This derivation involves only very simple and biologically plausible reactions, such as decarboxylation, oxidation, and... 

The decarboxylative arylation of potassium oxalate monoesters also occurs to give the corresponding aromatic esters (Scheme 4.68) [70]. The decarboxylative oxidative coupling of a-keto carboxylic acids with aryltrifluoroborates takes place in the presence of a palladium catalyst together with (NH4)2S20g as oxidant (Scheme 4.69) [71]. a-lmino carboxylates also undergo decarboxylative... 

This ladical-geneiating reaction has been used in synthetic apphcations, eg, aioyloxylation of olefins and aromatics, oxidation of alcohols to aldehydes, etc (52,187). Only alkyl radicals, R-, are produced from aliphatic diacyl peroxides, since decarboxylation occurs during or very shortiy after oxygen—oxygen bond scission in the transition state (187,188,199). For example, diacetyl peroxide is well known as a source of methyl radicals (206). 

Benzoic acid [65-85-0] C H COOH, the simplest member of the aromatic carboxyHc acid family, was first described in 1618 by a French physician, but it was not until 1832 that its stmcture was deterrnined by Wn b1er and Liebig. In the nineteenth century benzoic acid was used extensively as a medicinal substance and was prepared from gum benzoin. Benzoic acid was first produced synthetically by the hydrolysis of benzotrichloride. Various other processes such as the nitric acid oxidation of toluene were used until the 1930s when the decarboxylation of phthaUc acid became the dominant commercial process. During World War II in Germany the batchwise Hquid-phase air oxidation of toluene became an important process. 

The approach makes use of a bipyrroledicarbaldehyde 54 and a tripyrranedicarboxylic acid 55 which are condensed with subsequent decarboxylation in the presence of acid and oxygen. The presence of oxygen, as in many other syntheses of porphinoid macrocycles, is necessary to adjust the oxidation level of the chromophore which is in sapphyrins a 2271-aromatic cyclically conjugated system. Many sapphyrins 56 with different substitution patterns have been synthesized according to this general scheme. As in all McDonald-type condensations at least one of the components has to be symmetric because otherwise mixtures of constitutional isomers would be formed. 

At elevated temperatures, methylene carbons cleave from aromatic rings to form radicals (Fig. 7.44). Further fragmentation decomposes xylenol to cresols and methane (Fig. 7.44a). Alternatively, auto-oxidation occurs (Fig. 1.44b ). Aldehydes and ketones are intermediates before decarboxylation or decarbonylation takes place to generate cresols and carbon dioxide. These oxidative reactions are possible even in inert atmospheres due to the presence of hydroxyl radicals and water.5... 

Substituted phenylacetic acids form Kolbe dimers when the phenyl substituents are hydrogen or are electron attracting (Table 2, Nos. 20-23) they yield methyl ethers (non-Kolbe products), when the substituents are electron donating (see also chap. 8). Benzoic acid does not decarboxylate to diphenyl. Here the aromatic nucleus is rather oxidized to a radical cation, that undergoes aromatic substitution with the solvent [145]. 

Reaction No. 5 (Table 11) is part of a synthetically useful method for the alkylation of aromatic compounds. At first the aromatic carboxylic acid is reductively alkylated by way of a Birch reduction in the presence of alkyl halides, this is then followed by an eliminative decarboxylation. In reaction No. 9 decarboxylation occurs probably by oxidation at the nitrogen to the radical cation that undergoes decarboxylation (see... 

Pseudo-Kolbe electrolysis is the name given to anodic decarboxylations where the electron transfer does not occur from the carboxylate but from a group attached to it [31]. These oxidations are characterized by potentials that are much lower than the critical potential for the Kolbe electrolysis. The salt of p-methoxyphenylacetic acid can be oxidized in methanol to afford the corresponding methyl ether as the sole product. The low oxidation potential of 1.4 V (see) suggests, that the electron is being transferred from the aromatic nucleus (Eq. 39) [31]. 

Despite its synthetic importance, the mechanism of the copper-quinoline method has been studied very little, but it has been shown that the actual catalyst is cuprous ion. In fact, the reaction proceeds much faster if the acid is heated in quinoline with cuprous oxide instead of copper, provided that atmospheric oxygen is rigorously excluded. A mechanism has been suggested in which it is the cuprous salt of the acid that actually undergoes the decarboxylation. It has been shown that cuprous salts of aromatic acids are easily decarboxylated by heating in quinoline and that arylcopper compounds are intermediates that can be isolated in some cases. Metallic silver has been used in place of copper, with higher yields. ... 

The reductive transformation of arene carboxylates to the corresponding aldehydes under aerobic conditions has already been noted. In addition, aromatic aldehydes may undergo both reductive and oxidative reactions, with the possibility of decarboxylation of the carboxylic acid formed ... 

The decarboxylation of carboxylic acid in the presence of a nucleophile is a classical reaction known as the Hunsdiecker reaction. Such reactions can be carried out sometimes in aqueous conditions. Man-ganese(II) acetate catalyzed the reaction of a, 3-unsaturated aromatic carboxylic acids with NBS (1 and 2 equiv) in MeCN/water to afford haloalkenes and a-(dibromomethyl)benzenemethanols, respectively (Eq. 9.15).32 Decarboxylation of free carboxylic acids catalyzed by Pd/C under hydrothermal water (250° C/4 MPa) gave the corresponding hydrocarbons (Eq. 9.16).33 Under the hydrothermal conditions of deuterium oxide, decarbonylative deuteration was observed to give fully deuterated hydrocarbons from carboxylic acids or aldehydes. 

As pointed out previously, controlled degradation reactions are very difficult with aliphatic or alicyclic hydrocarbons, and most of the relabeling work has been concentrated on aromatic reaction products. Procedures have been extensively described by Pines and co-workers (e.g., 97, 96, also 87, 89-98, 95, 98). For the present purpose, it suffices to note that the 14C contents of the methyl side-chains and the rings in aromatic reaction products are readily estimated by oxidation of the methyl to carboxyl, followed by decarboxylation, while ethyl side-chains may be oxidatively degraded one carbon atom at a time. Radiochemical assays may be made on CO2 either directly in a gas counter, or after conversion to barium carbonate, while other solid degradation intermediates (e.g., benzoic acid or the phthalic acids) may be either assayed directly as solids or burned to CO2. Liquids are best assayed after burning to CO2. 

The low specificity of electron-donating substrates is remarkable for laccases. These enzymes have high redox potential, making them able to oxidize a broad range of aromatic compounds (e.g. phenols, polyphenols, methoxy-substituted phenols, aromatic amines, benzenethiols) through the use of oxygen as electron acceptor. Other enzymatic reactions they catalyze include decarboxylations and demethylations [66]. 

Several processes often occur in lipids, including oxidation, hydration, dehydration, decarboxylation, esterification, aromatization, hydrolysis, hydrogenation and polymerization. In fact, the chemistry of these materials can be affected, for example, by heat (anthropogenic transformations), humidity, pH, and microbial attacks. 

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. 

Dopamine synthesis in dopaminergic terminals (Fig. 46-3) requires tyrosine hydroxylase (TH) which, in the presence of iron and tetrahydropteridine, oxidizes tyrosine to 3,4-dihydroxyphenylalanine (levodopa.l-DOPA). Levodopa is decarboxylated to dopamine by aromatic amino acid decarboxylase (AADC), an enzyme which requires pyri-doxyl phosphate as a coenzyme (see also in Ch. 12). 

Insertion of aUcynes into aromatic C-H bonds has been achieved by iridium complexes. Shibata and coworkers found that the cationic complex [Ir(COD)2]BF4 catalyzes the hydroarylation of internal alkynes with aryl ketones in the presence of BINAP (24) [111]. The reaction selectively produces ort/to-substituted alkenated-aryl products. Styrene and norbomene were also found to undergo hydroarylation under similar condition. [Cp IrCl2]2 catalyzes aromatization of benzoic acid with two equivalents of internal alkyne to form naphthalene derivatives via decarboxylation in the presence of Ag2C03 as an oxidant (25) [112]. 

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