Hydroxylation NIH shift

Evidence for the direct oxidation of benzene (or substituted benzenes) to benzene oxide (or substituted benzene oxides) by enzymatic (Refs. 5 and 35 and references therein) and chemical (Refs, 35 and 36 and references therein) methods is available both from the observation of the migration and retention of ring substituents during aromatic hydroxylation (NIH shift),and from the nature of the isolated products (phenols, rans-dihydrodiols). As a direct consequence of its thermal instability and high reactivity, benzene oxide 1 has not yet been isolated as an oxidation product of benzene. 

System Athene epoxidation S NS Alkane hydroxylation S NS Arene hydroxylation NIH shift Athene ketonization R s. 

In addition to nonheme iron complexes also heme systems are able to catalyze the oxidation of benzene. For example, porphyrin-like phthalocyanine structures were employed to benzene oxidation (see also alkane hydroxylation) [129], Mechanistic investigations of this t3 pe of reactions were carried out amongst others by Nam and coworkers resulting in similar conclusions like in the nonheme case [130], More recently, Sorokin reported a remarkable biological aromatic oxidation, which occurred via formation of benzene oxide and involves an NIH shift. Here, phenol is obtained with a TON of 11 at r.t. with 0.24 mol% of the catalyst. 

Recently, the mechanism of 6-nitro-BaP ring hydroxylation has been elucidated by using 3-deutero-6-nitro-BaP (144). When incubated with 3-methylcholanthrene-induced rat liver microsomes, this deuterated analogue yielded the same metabolite profile previously observed with 6-nitro-BaP. Spectroscopic analysis of 3-hydroxy-6-nitro-BaP and 6-nitro-BaP-3,9-hydroquinone indicated that 30% of the deuterium label had migrated to carbon 2, presumably via an NIH shift. Therefore, it appears that 6-nitro-BaP-2,3-oxide is a common intermediate for these two metabolites. 

The concept of microbial models of mammalian metabolism was elaborated by Smith and Rosazza for just such a purpose (27-32). In principle, this concept recognizes the fact that microorganisms catalyze the same types of metabolic reactions as do mammals (32), and they accomplish these by using essentially the same type of enzymes (29). Useful biotransformation reactions common to microbial and mammalian systems include all of the known Phase I and Phase II metabolic reactions implied, including aromatic hydroxylation (accompanied by the NIH shift), N- and O-dealkylations, and glucuronide and sulfate conjugations of phenol to name but a few (27-34). All of these reactions have value in studies with the alkaloids. 

Reinhold and Bruni studied the metabolism of 7,9-dideuterioellipticine (17) in rats and found that deuterium originally at position 9 was completely lost during the mammalian hydroxylation process (147). Proton and carbon-13 NMR and mass spectral analyses confirmed the complete elimination of deuterium at position 9, thus ruling out the occurrence of an NIH shift mechanism in the hydroxylation of ellipticine. An oxygen-insertion process was rationalized to account for the mechanism of aromatic hydroxylation in rats since this would not be expected to display the NIH shift but should demonstrate an isotope effect. It was... 

The NIH shift has been found to occur during aromatic hydroxylations catalyzed by enzymes present in plants, animals, fungi and bacteria. It is thus evident that the acid catalyzed (or spontaneous) isomerization of oxepins-arene oxides is a very important type of in vivo reaction. It should be emphasized that the NIH shift may occur under either acid-catalyzed or neutral (spontaneous) conditions (76ACR378). The direct chemical oxidation of aromatic rings has also yielded both phenols (obtained via the NIH shift) and arene oxides (80JCS(P1)1693>. 

The NIH shift in the hydroxylation of Trp by TPH is known to occur from carbon 5 to carbon 4 exclusively (70,140). However, the NIH shift for indole in the H0-FeIV=0 and [H20-FeIV=0]+ models showed no preference for migration of the hydride to carbon 4 over carbon 6, which was claimed to be caused by the lack of steric preference exerted by the active site models compared to that of the actual enzymes (117). 

This hydroxylation-induced intramolecular migration, known as the NIH shift, was explained by the involvement of arene oxides formed by the attack of electrophilic oxoiron(V) porphyrin on the aromatic ring.753 Intermediate 98 was also suggested to be formed in hydroxylation by the Fenton and related reagents in aprotic media after initial oxidation with an oxoiron(V) complex followed by electron transfer.744 754... 

Recently, the PCB-biodegradative capabilities of methanotrophs have been demonstrated (Adriaens, 1994). In this study, 2-CB was oxidized by a methanotrophic culture (CSC1) to a hydroxylated chlorobiphenyl intermediate identified as 2-hydroxy-3-chlorobiphenyl. This intermediate indicated that the metabolite was formed via a concerted oxidation involving an arene oxide which rearranges spontaneously via an NIH shift. No studies have shown, however, that methanotrophs can degrade more highly chlorinated PCBs, and their utility for bioremediation processes does not seem promising. 

NADH-dependent reductase, thus allowing the biopterin cofactor to function catalytically (72JBC(247)6082). That the conversion of phenylalanine to tyrosine involves an arene oxide intermediate is suggested by the observation of the so-called NIH shift phenomenon (i.e. migration and retention of the para substituents such as deuterium, tritium, methyl and bromine when these para-substituted phenylalanines are enzymatically hydroxylated) <66BBR(24)720, 67MI11000). 

Operation of the NIH shift can cause migration of a large substituent as is illustrated by the hydroxylation of 4-hydroxyphenylpyruvate (Eq. 18-49), a key step in the catabolism of tyrosine (Chapter 25). Human 4-hydroxyphenylpyruvate dioxygenase is a dimer of 43-kDa subunits.439 A similar enzyme from Pseudomonas is a 150-kDa tetrameric iron-tyrosinate protein, which must be maintained in the reduced Fe(II) state for catalytic activity.440 Although this enzyme is a... 

In mammalian liver microsomes, cytochrome P-450 is not specific and catalyzes a wide variety of oxidative transformations, such as (i) aliphatic C—H hydroxylation occurring at the most nucleophilic C—H bonds (tertiary > secondary > primary) (ii) aromatic hydroxylation at the most nucleophilic positions with a characteristic intramolecular migration and retention of substituents of the aromatic ring, called an NIH shift,74 which indicates the intermediate formation of arene oxides (iii) epoxidation of alkenes and (iv) dealkylation (O, N, S) or oxidation (N, S) of heteroatoms. In mammalian liver these processes are of considerable importance in the elimination of xenobiotics and the metabolism of drugs, and also in the transformation of innocuous molecules into toxic or carcinogenic substances.75 77... 

Aromatic hydrocarbons are mainly hydroxylated to phenolic products. Complex (12) hydroxylated benzene in MeCN at 20 °C into phenol in ca. 55% yield, and no isotope effect was found for this reaction. Hydroxylation of toluene mainly occurs at the ring positions, with minor amounts of benzylic oxidation products. Hydroxylation of 4-deuterotoluene by (12) occurred with 70% retention and migration of deuterium in the formation of p-cresol. This high NIH shift value is in the same range as that found for liver microsome cytochrome P-450 hydroxylase, and suggests the transient formation of arene oxide intermediates. 

Institute of Health) shift.80,110,111 Originally, the term NIH shift was used as a phenomenological description of the consequence of hydroxylation of aromatic compounds by mixed-function oxygenases. These enzymes catalyze the oxidation of aromatic substrates by deriving oxygen from molecular oxygen and not from water.80,110,111 Later studies narrowed the term to include arene oxide involvement.80... 

The NIH shift has been recognized to be so general that whenever a 1,2-shift occurs in aromatic hydroxylation reactions, it is assumed that arene oxides are involved. This need not be so. That the 1,2-shift could take place without the... 

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