Reductive dehalogenation reaction compound

As pointed out earlier a third class of B12-dependent enzymes, present in anaerobic microbes, carry out reductive dehalogenation reactions, which play an important role in the detoxification of chlorinated aliphatic and aromatic compounds, among which are many important man-made pollutants. The role of B12 in this class of enzymes is not clear— possibly by formation of an organocobalt adduct, as in the case of methyltransferases or alternatively by the corrinoid serving as an electron donor. 

Reductive dehalogenation reactions catalyzed by P-450 have been studied extensively, primarily because of the interest in compounds such as anesthetics, pesticides, and potentially toxic industrial solvents. An anesthetic named halothane gives anion-radical that undergoes dehalogenation according to the following equation ... 

Consequently, with the present knowledge of reductive dehalogenation reactions of Cr and C2-compounds, and considering the quality of the various molecular descriptors, only qualitative, or at most semiquantitative, predictions of the relative reactivities of a confined set of structurally related compounds in a given system are possible. Nevertheless, evaluation of such relative reactivities in different systems may provide important insights into such reactions, which will be demonstrated by the following two examples. These two examples will, however, also illustrate the... 

Why is it so difficult to derive generally applicable quantitative structure-reactivity relationships (QSARs) for redox reactions involving organic compounds What is particularly problematic when dealing with reductive dehalogenation reactions ... 

Five catalyst types were used in these product distribution studies Pd/C, Pd/alumina, pure Pd metal powder, Pd/Fe, and Pd/Cu/support. The last two catalysts are not traditional materials. The Pd/Cu, which was used in the reduction of nitrate, was a bimetallic catalyst on an alumina, silica, or polymer support. Fe is an atypical support in that it has the intrinsic ability to reductively dehalogenate chlorinated compounds by oxidizing to Fe2+ however, the rapid reaction rates associated with Pd/Fe are indicative of Pd-catalyzed reactions, which are much faster than Fe reactions. 

Reductive Dehalogenation Reactions of Halogenated Aliphatic and Alicyclic Compounds... 

Two important examples of reductive metabolism of xenobiotics are the reductive dehalogenation of organohalogen compounds, and the reduction of nitroaromatic compounds. Examples of each are shown in Figure 2.13. Both types of reaction can take place in hepatic microsomal preparations at low oxygen tensions. Cytochrome P450 can catalyze both types of reduction. If a substrate is bound to P450 in the... 

Reductive dehalogenation cannot be completely controlled, and mostly complicated mixtures were formed which are difficult to separate. Salt elimination opens the possibility of a reaction aimed at polysilane formation. Some examples are shown in Fig. 2. The key compounds are the alkali metal cyclosilanes, which we have isolated via the mercury compounds by the action of sodium/potassium alloy and used for the first time [13]. 

In a similar type of reaction, polymer-supported hydridoiron tetracarbonyl anion reacts with simple non-benzylic aliphatic bromides and iodides to produce aldehydes (Table 8.15), presumably through the intermediate formation of RCOFeH(CO)3, which undergoes reductive extrusion of the aldehydes [3], In contrast, benzylic halides and a-halocarbonyl compounds are reductively dehalogenated by the HFe(CO)4 anion (see Chapter 11). 

Organochalcogen(II) compounds, 100-102 Organochalcogen(IV) compounds, 100-102 Organoselenium compounds dehalogenation reactions, 96 electrochemical reduction, 113-117 haloperoxidase-like activity, 108-113 with odd number of ligands, 100-102 one-electron oxidation, 117-118 oxidation of thiols, 102-106 redox reactions, 79-80 thioperoxidase-like activity, 108-113 Organotellurium compounds... 

In the following we will try to illustrate these general points by discussing two specific types of redox reactions the reduction of aromatic nitro groups (Eq. 14-9) and the reductive dehalogenation of polyhalogenated Cr and C2-compounds (Eqs. 14-6 to 14-8). These two cases represent two very different types of reactions. In the first case, the transfer of the first electron is reversible, whereas in the second case, it is typically irreversible and involves the breaking of a bond. In the latter case, therefore, one speaks of a dissociative electron transfer. Furthermore, compounds... 

In summary, the overall rate of reductive dehalogenation of a given compound in a given system may be determined by various rather complex steps, and may, therefore, be influenced by several compound properties. Furthermore, even within a series of structurally related compounds, the relative importance of the various steps may differ, thus rendering any quantitative structure reactivity relationships (QSARs) rather difficult. This also means that calibration of a given system with a small set of model compounds for estimating absolute reaction rates will be even more difficult as compared to the situation with NAC reduction (see above). 

Try to explain qualitatively the observed differences in reactivity. Are there compounds in this table for which other reactions than reductive dehalogenation may be important under these conditions If yes, which ones, and what kind of reaction do they undergo ... 

Dihalocydopropanes readily undergo reductive dehalogenation under a variety of conditions. Suitable choice of reagents and reaction conditions will allow the synthesis of monohalocyclopropanes or the parent cyclopropanes.19 " The ease of reduction follows the expected order I > Br > Cl > F. In general, complete reduction of dibromo and dichloro compounds is accomplished by alkali metal in alcohol,99-102 liquid ammonia103 or tetrahydrofuran (equations 28 and 29).104 The dihalocydopropanes can be reduced conveniently with LAH (equation 30).105 LAH reduction is particularly suited for difluoro compounds which are resistant to dissolving metal reductions.19 106 It is noteworthy that the sequence of dihalocar-bene addition to an alkene followed by the reduction of the dihalocyclopropyl compounds (equation 31) provides a convenient and powerful alternative to Simmons-Smith cyclopropanation, which is not always reliable. 

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