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Vitamin B12, reactions

New developments in the field of vitamin B12 reactions of the cobalt atom in corrins and vitamin B12 model compounds. G. N. Schrauzer, Angew. Chem., Int. Ed. Engl., 1976,15, 417-426 (67). [Pg.56]

There are more complex examples of metal ion catalysis. Cobalt in vitamin B12 reactions forms covalent bonds with carbons of substrates.41,42 Metals can also act as electron conduits in redox reactions. For example, in cytochrome c the iron in the heme is reversibly oxidized and reduced. [Pg.376]

Murakami Y, Hisaeda Y, Ozaki T, Tashiro T, Ohno T, Tani Y, Matsuda Y (1987) Hydrophobic vitamin B12. V. Electrochemical carbon-skeleton rearrangement as catalyzed by hydrophobic vitamin B12 reaction mechanisms and migratory aptitude of functional groups. Bull Chem Soc Jpn 60 311-324... [Pg.821]

Scheme 1 outlines the retrosynthetic analysis of the Woodward-Eschenmoser A-B variant of the vitamin B12 (1) synthesis. The analysis begins with cobyric acid (4) because it was demonstrated in 1960 that this compound can be smoothly converted to vitamin B12.5 In two exploratory corrin model syntheses to both approaches to the synthesis of cobyric acid,6 the ability of secocorrinoid structures (e. g. 5) to bind metal atoms was found to be central to the success of the macrocyclization reaction to give intact corrinoid structures. In the Woodward-Eschenmoser synthesis of cobyric acid, the cobalt atom situated in the center of intermediate 5 organizes the structure of the secocorrin, and promotes the cyclization... [Pg.100]

In /(-cormorsterone (14), we have an intermediate that possesses all six contiguous stereogenic centers occupying the left-hand portion of vitamin B12. Scheme 7 presents the straightforward and elegant sequence of reactions that led to the synthesis of cyanobro-mide 6, and the observations that formed the basis for this... [Pg.110]

Scheme 8 presents the sequence of reactions that led to the synthesis of the B-ring of vitamin B12 by the Eschenmoser group. An important virtue of the Diels-Alder reaction is that it is a stereospecific process wherein relative stereochemical relationships present in the diene and/or the dienophile are preserved throughout the course of the reaction.8 Thus, when the doubly activated dienophile 12 (Scheme 8) is exposed to butadiene 11 in the presence of stannic chloride, a stereospecific reaction takes place to give compound 27 in racemic form. As expected, the trans relationship between... [Pg.113]

Vitamin B12. Figure 2 Selected reactions in which folic acid coenzymes are involved. [Pg.1292]

Mild diarrhea and itching have been reported with the administration of vitamin B12. Other adverse reactions that may be seen include a marked increase in RBC production, acne, peripheral vascular thrombosis, congestive heart failure, and pulmonary edema... [Pg.437]

Lactic acidosis (buildup of lactic acid in the blood) may also occur with die administration of metformin. Although lactic acidosis is a rare adverse reaction, its occurrence is serious and can be fatal. Lactic acidosis occurs mainly in patients with kidney dysfunction. Symptoms of lactic acidosis include malaise (vague feeling of bodily discomfort), abdominal pain, rapid respirations, shortness of breath, and muscular pain. In some patients vitamin B12 levels are decreased. This can be reversed with vitamin B12 supplements or with discontinuation of the drug therapy. Because... [Pg.503]

Much research focuses on the structures, properties, and uses of the complexes formed between d-metal ions acting as Lewis acids and a variety of Lewis bases, partly because they participate in many biological reactions. Hemoglobin and vitamin B12, for example, are both complexes—the former of iron and the latter of cobalt (Box 16.1). Complexes of the d-metals are often brightly colored and magnetic and are used in chemistry for analysis, to dissolve ions (Section 11.13), in the... [Pg.788]

The replacement of the O—H O bridges with BF2 of BPh2 may affect both the complex geometry [178] and the electron density at the central metal ion [184], providing the opportunity of adjusting the Co—C bond strength towards homolytic cleavage, which is currently accepted to be the first step of the reactions catalyzed by the vitamin B12 coenzyme [185]. [Pg.36]

Ragsdale, S. W. Kumar, M. Zhao, S. Menon, S. Seravalli, J. Doukov, T. Discovery of a Bio-organometallic Reaction Sequence Involving Vitamin B12 and Nickel/ Iron-Sulfur Clusters Wiley-VCH Weinheim, Germany, 1998. [Pg.327]

The ITIES with an adsorbed monolayer of surfactant has been studied as a model system of the interface between microphases in a bicontinuous microemulsion [39]. This latter system has important applications in electrochemical synthesis and catalysis [88-92]. Quantitative measurements of the kinetics of electrochemical processes in microemulsions are difficult to perform directly, due to uncertainties in the area over which the organic and aqueous reactants contact. The SECM feedback mode allowed the rate of catalytic reduction of tra 5-l,2-dibromocyclohexane in benzonitrile by the Co(I) form of vitamin B12, generated electrochemically in an aqueous phase to be measured as a function of interfacial potential drop and adsorbed surfactants [39]. It was found that the reaction at the ITIES could not be interpreted as a simple second-order process. In the absence of surfactant at the ITIES the overall rate of the interfacial reaction was virtually independent of the potential drop across the interface and a similar rate constant was obtained when a cationic surfactant (didodecyldimethylammonium bromide) was adsorbed at the ITIES. In contrast a threefold decrease in the rate constant was observed when an anionic surfactant (dihexadecyl phosphate) was used. [Pg.321]

Lenhert and Hodgkin (15) revealed with X-ray diffraction techniques that 5 -deoxyadenosylcobalamin (Bi2-coenzyme) contained a cobalt-carbon o-bond (Fig. 3). The discovery of this stable Co—C-tr-bond interested coordination chemists, and the search for methods of synthesizing coen-zyme-Bi2 together with analogous alkyl-cobalt corrinoids from Vitamin B12 was started. In short order the partial chemical synthesis of 5 -de-oxyadenosylcobalamin was worked out in Smith s laboratory (22), and the chemical synthesis of methylcobalamin provided a second B 12-coenzyme which was found to be active in methyl-transfer enzymes (23). A general reaction for the synthesis of alkylcorrinoids is shown in Fig. 4. [Pg.54]

Vitamin B12 derivatives are also effective catalysts for the electroreductive cyclization of bromoalkenes in conductive microemulsions,299 300 or for ring-expansion reactions in cyclic a-(bromomethyl)-(3-keto esters in DMF.301 Vitamin Bi2 attached to an epoxy-polymer has been used in electrosynthesis of valeronitrile by reductive coupling of iodoethane and acrylonitrile.302... [Pg.489]

Homocystinuria Usually a failure of cystathionine synthase (Fig. 40-2 reaction 6). Rarely associated with aberrant vitamin B12 metabolism (Fig. 40-2) Thromboembolic diathesis, marfanoid habitus, ectopia lentis. Mental retardation is frequent. Diet low in methionine Vitamin B6 in pyridoxine-responsive syndromes Vitamin B12 in responsive syndromes Anticlotting agents... [Pg.668]

On rare occasions an organic aciduria occurs not because of an enzyme deficiency but from a failure to transport or activate a water-soluble vitamin that serves as a cofactor for the reaction in question. Thus, congenital deficiencies in the metabolism of vitamin B12 commonly give rise to methylmalonic aciduria (Fig. 40-1, Table 40-2). Similarly, deficiencies of biotin metabolism can cause a severe organic aciduria (Table 40-2). It is very important to be aware of the defects of vitamin metabolism because the administration of large doses of these cofactors may completely prevent brain damage. [Pg.669]


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See also in sourсe #XX -- [ Pg.203 ]




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