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Nicotinamide chemical synthesis

Because the resolution with acylase gave a theoretical maximum yield of only 50% and required separation of the desired product from the unreacted enantiomer at the end of the reaction, we next tried to prepare the amino acid by reductive amination of the corresponding ketoacid, a process with a theoretical maximum yield of 100%. A variety of ketoacids can be converted to L-amino acids by treatment with ammonia, reduced nicotinamide adenine dinucleotide (NADH), and a suitable amino acid dehydrogenase. 2-Keto-6-hydroxyhexanoic acid (in equilibrium with its cyclic hemiketal form) was prepared by chemical synthesis starting from 4-chloro-l-butanol, which was... [Pg.281]

Chemical Synthesis of Nicotinamide in Heat-Sterilization of Culture... [Pg.106]

As mentioned in Chapter 1 the same Rhodococcus rhodochrous catalyses the last step in Lonza s >3500 tonnes/year nicotinamide synthesis [94, 111, 112]. Lonza has further developed this technology and currently synthesises a number of relevant fine chemical building blocks with nitrile hydratases [94, 113]. [Pg.288]

Introduction. The work to he reviewed will concern the mechanism and pathways of synthesis of adrenal corticosteroids as they may he affected hy the natural hormone, ACTH, and various chemical agents. For the purpose of orientation an outline of the pathways of synthesis is included helow. The solid arrows indicate the need for O2 and reduced nicotinamide... [Pg.263]

Simple procedures for the preparation of NMN+ by chemical or enzymic methods have been reported and although the phosphorylating agent metaphosphoric acid used in the chemical phosphorylation of nicotinamide 2, 3 -0-isopropylidene ribofuranoside is relatively imsophisticated, the synthesis can be carried out on a large scale with moderate yields. The stereo-... [Pg.124]

In contrast to the chemical alkaline hydrolysis of 3-cyanopyridine with 4% byproduct of nicotinic acid (96% yield) the biotransformation works with absolute selectivity and no acid or base is required. The biotransformation (a continuous process) is operated at low temperature and atmospheric pressure. In contrast to the old synthesis route of nicotinamide at Lonza, the new one is environmentally friendly and safe. There is only one organic solvent used throughout the whole process in four highly selective continuous and catalytic reactions. The process water, NH3 and H2 are recycled. [Pg.1451]

We propose that conditions altering the availability of NAD may be signaled to chromatin by the intermediacy of poly(ADP-ribose) (Fig. 2). The question is whether this signal operates imder physiological conditions. Some reports have provided direct evidence that NAD- depletion forced upon cells by incubation in nicotinamide-free medium, arrests poly(ADP-ribose) synthesis (5) and drastically alters chromatin functions (5-7). For example, DNA repair in response to a chemical carcinogen was arrested under these conditions, but could be reestablished with nicotinamide, which restored normal intracellular NAD- and poly(ADP-ribose) levels (5). Similarly, myoblast differentiation was reversibly inhibited either by nicotinamide starvation or by selective inhibition of poly(ADP-ribose) polymerase (7). These results illustrate that nutritional manipulation of... [Pg.215]

Jagodzinski PW, Peticolas WL (1981) Resonance enhanced Raman identification of the zinc-oxygen bond in a horse liver alcohol dehydrogenase-nicotinamide adenine dinucleotide-aldehyde transient chemical intermediate. J Am Chem Soc 103 234-236 Jakovac IJ, Goodbrand HB, Lok KP, Jones JB (1982) Enzymes in organic synthesis. 24. Preparations of enantiomerically pure chiral lactones via stereospecific horse liver alcohol dehydrogenase... [Pg.97]

Nifrilases are emerging as an important tool in industrial synthesis of bulk chemicals and the production of pharmaceuticals and pharmaceutical intermediates. Acrylamide (17) and nicotinamide (18) are produced with the help of a nitrile hyc tase (19). Fiuthermore the organinc solvent 1,5-dimethyl-2-piperidone is produced using a nifrilase (20). High selectivity and... [Pg.53]


See other pages where Nicotinamide chemical synthesis is mentioned: [Pg.136]    [Pg.185]    [Pg.370]    [Pg.270]    [Pg.47]    [Pg.9]    [Pg.298]    [Pg.169]    [Pg.507]    [Pg.148]    [Pg.294]    [Pg.4]    [Pg.189]    [Pg.197]    [Pg.507]    [Pg.162]    [Pg.100]    [Pg.270]    [Pg.282]    [Pg.656]    [Pg.344]    [Pg.201]    [Pg.658]    [Pg.140]    [Pg.94]    [Pg.67]    [Pg.273]    [Pg.70]   
See also in sourсe #XX -- [ Pg.185 ]




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Nicotinamide synthesis

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