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Books on the topic 'Synthesis of nitrosyl compound'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 February 2022

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1

Rubenchik, Boris Lʹvovich. Obrazovanie kant͡s︡erogenov iz soedineniĭ azota. Kiev: Nauk. dumka, 1990.

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2

Keller, Antoni. Kompleksy nitrozylowe molibdenu w syntezie organicznej: Reakcje metatezy, polimeryzacji i izomeryzacji olefin. Wrocław: Wydawn. Uniwersytetu Wrocławskiego, 1993.

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3

Vermerris, Wilfred. Phenolic compound biochemistry. Dordrecht: Springer, 2008.

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4

Jones, Anthony C. CVD of compound semiconductors: Precursor synthesis, development and applications. Weinheim, Germany: VCH, 1997.

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5

M, Villalgordo José, ed. Solid-supported combinatorial and parallel synthesis of small-molecular-weight compound libraries. [New York]: Pergamon, 1998.

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6

Soares-Sello, Anna Mampe. Synthesis of a potential DNA binding compound containing the 2-arylindole ring system. Norwich: University of East Anglia, 1991.

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7

Symposium C on High Energy Ion Implantation (1991 Strasbourg, France). High energy and high dose ion implantation: Proceedings of Symposium C on High Energy Ion Implantation and Symposium D on Ion Beam Synthesis of Compound and Elemental Layers of the 1991 E-MRS Spring Conference, Strasbourg, France, May 28-31, 1991. Amsterdam: North-Holland, 1992.

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8

Vermerris, Wilfred, and Ralph Nicholson. Phenolic Compound Biochemistry. Springer, 2008.

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9

O'Brien, Paul, and Anthony C. Jones. CVD of Compound Semiconductors: Precursor Synthesis, Developmeny and Applications. Wiley & Sons, Incorporated, John, 2008.

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10

O'Brien, Paul, and Anthony C. Jones. CVD of Compound Semiconductors: Precursor Synthesis, Developmeny and Applications. Wiley & Sons, Limited, John, 2008.

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11

Solid-Supported Combinatorial and Parallel Synthesis of Small-Molecular-Weight Compound Libraries. Elsevier, 1998. http://dx.doi.org/10.1016/s1460-1567(98)x8025-6.

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12

Schlunegger, Urs Peter. Biologically Active Molecules: Identification, Characterization and Synthesis : Proceedings of a Seminar on Chemistry of Biologically Active Compound. Springer, 1989.

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13

Postma, James M., J. Leland Hollenberg, and Julian Roberts. Synthesis of a Chemical Compound: Making Alum from an Aluminum Can: Separate from Chemistry in the Laboratory 5e. W. H. Freeman, 2000.

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14

Dierdorf, Stephen F. Porphyria. Edited by Matthew D. McEvoy and Cory M. Furse. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190226459.003.0026.

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Heme, and iron containing compound that forms the nonprotein portion of hemoglobin, is essential to life. Heme synthesis requires eight enzymatic steps, and a deficiency in any one of the eight enzymes can lead to the accumulation of potentially toxic intermediates. Some forms of porphyria may be asymptomatic until the patient receives a triggering agent, and acute porphyrias can also be difficult to diagnose because of the nonspecific clinical features. The most serious of the clinical manifestations is severe neurologic dysfunction. An attack can be triggered by medications administered during the perioperative period, and failure to act promptly can result in mortality rates as high as 5%.
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15

Cheillan, David, and Frédéric Sedel. Disorders of Creatine Metabolism. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0010.

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Creatine is a physiological guanidino compound playing a major role in energy metabolism in muscle and implicated in neurotransmission in brain. The three disorders of creatine metabolism (AGAT and GAMT deficiencies and the X-linked creatine transporter defect) are a group of inborn errors of metabolism characterized by a depletion of creatine that could be easily diagnosed by mesasurement of guanidinoacetate and creatine in body fluid or cranial MRS spectroscopy. The main clinical features of these paediatric disorders are intellectual disability and speech delay and some adult patients have been described with severe language impairment and mental retardation. Although the X-linked creatine transporter defect is currently not treatable, the clinical symptoms of the two disorders of creatine synthesis should be improved by creatine supplementation emphasizing the importance of an early diagnostic.
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