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Libri sul tema "Phosphine – Synthesis"

Autore: Grafiati
Pubblicato: 4 giugno 2021
Ultima modifica: 10 febbraio 2022

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1

Wiktelius, Daniel. Asymmetric synthesis of dipeptidomimetics and phosphine-boranes: Routes involving stereoselective olefination, expoxidation, and lipase-catalysed reactions. Göteborg: Göteborg University, 2007.

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2

Yaluma, A. K. Novel chiral phosphines for asymmetric synthesis. Manchester: UMIST, 1995.

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3

Butt, Afshan Hena. Syntheses of analogues of some important phosphate esters. Birmingham: University of Birmingham, 2001.

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4

Lee, Sam. Synthesis and characterization of fluorescent-labelled oligoglycols by the phosphite-triester method. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1991.

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5

Calcium phosphates in oral biology and medicine. Basel: Karger, 1991.

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6

Toivari, Mervi. Engineering the pentose phosphate pathway of Saccharomyces cerevisiae for production of ethanol and xylitol. [Espoo, Finland]: VTT Technical Research Centre of Finland, 2007.

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7

Healy, Christopher. Synthetic studies on the inhibition of L-myo-inositol 1-phosphate synthase. Birmingham: University of Birmingham, 1991.

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8

Kürkçüogľu, Išin. The effect of staphylococci on the dissolution of synthetic calcium phosphate biomaterials. Birmingham: University of Birmingham, 2001.

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9

Tan, Chui Heong. Synthetic studies on the inhibition of L-myo-inositol-1-phosphate synthase. Birmingham: University of Birmingham, 1994.

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10

Liu, George Zhigang. Studies on itaconyl bis (sodium methyl phosphate) cross-linked hemoglobin and the synthesis of acyl methyl phosphonates. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1993.

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11

Johnson, A. William. Ylides and imines of phosphorus. New York: Wiley, 1993.

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12

Petrone, David A. Stereoselective Heterocycle Synthesis via Alkene Difunctionalization: Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation. Springer, 2018.

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13

Petrone, David A. Stereoselective Heterocycle Synthesis via Alkene Difunctionalization: Bulky Phosphine Ligands Enable Pd-Catalyzed Arylhalogenation, Arylcyanation and Diarylation. Springer, 2019.

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14

Heimann, R. B. Calcium phosphate: Structure, synthesis, properties, and applications. 2012.

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15

Heimann, Robert B. Calcium Phosphate: Structure, Synthesis, Properties, and Applications. Nova Science Publishers, Incorporated, 2014.

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16

Sereda, Julie Lenora. Synthesis, characterization and study of pyrrolyl and indolyl phosphines. 2001.

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17

Iron Phosphate: Production and Their Uses in Organic Synthesis. Nova Science Publishers, Incorporated, 2019.

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18

Wainwright, Matthew. P-N bond forming reactions for the synthesis of phosphines. 2000.

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19

Pearl, Phillip L., e William P. Welch. Pediatric Neurotransmitter Disorders. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0059.

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Abstract (sommario):
The pediatric neurotransmitter disorders represent an enlarging group of neurological syndromes characterized by inherited abnormalities of neurotransmitter synthesis, metabolism, and transport. Disorders involving monoamine synthesis include guanosine triphosphate cyclohydrolase deficiency (Segawa disease or classical Dopa-responsive dystonia as the heterozygous form), aromatic amino acid decarboxylase deficiency, tyrosine hydrolase deficiency, sepiapterin reductase deficiency, and disorders of tetrahydrobiopterin synthesis. These disorders can be classified according to whether they feature elevated serum levels of phenylalanine. Disorders of γ-amino butyric acid (GABA) metabolism include succinic semialdehyde dehydrogenase deficiency and GABA-transaminase deficiency. Glycine encephalopathy is typically manifested by refractory neonatal seizures due to a defect in the glycine degradative pathway. Pyridoxine-responsive seizures have now been associated with deficiency of α-aminoadipic semialdehyde dehydrogenase as well as a variants requiring therapy with pyridoxal-5-phosphate and folinic acid.
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20

Youm, Ji Youn. 1. Design and synthesis of phosphino-sulfonamide ligands. 2. Transition metal-catalyzed transformations of enamides and related compounds. 2005.

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21

United States. National Aeronautics and Space Administration., a cura di. Phospha-s-triazines and related compositions of improved hydrolytic and thermal stability. [Washington, DC: National Aeronautics and Space Administration, 1996.

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22

United States. National Aeronautics and Space Administration., a cura di. Phospha-s-triazines and related compositions of improved hydrolytic and thermal stability. [Washington, DC: National Aeronautics and Space Administration, 1996.

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23

United States. National Aeronautics and Space Administration., a cura di. Phospha-s-triazines and related compositions of improved hydrolytic and thermal stability. [Washington, DC: National Aeronautics and Space Administration, 1996.

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24

Rampersad, Nicole Claudia. New indolyl phosphines: Synthesis and characterization of 2-diphenylphosphine-3-methylindole and di(1H-3-indolyl)methane-(2,12)-phenylphosphine : . 2001.

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25

Wagner, Carsten A., e Olivier Devuyst. Renal acid–base homeostasis. A cura di Robert Unwin. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0024.

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Abstract (sommario):
The kidney is central to acid–base homeostasis. Major processes are reabsorption of filtered bicarbonate, de novo synthesis of bicarbonate from ammoniagenesis, and net excretion of protons. The latter requires buffers such as ammonium, phosphate, citrate and other bases binding protons (so-called titratable acids). The proximal tubule is the major site of bicarbonate reabsorption and only site of ammoniagenesis. The thick ascending limb and the distal convoluted tubule handle ammonia/ammonium and complete bicarbonate reabsorption. The collecting duct system excretes protons and ammonium, but may switch to net bicarbonate secretion. The kidney displays a great plasticity to adapt acid or bicarbonate excretion. Angiotensin II, aldosterone and endothelin are involved in regulating these processes, and they induce morphological changes along the nephron. Inborn and acquired disorders of renal acid–base handling are caused by mutations in acid–base transport proteins or by dysregulation of adaptive mechanisms.
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26

Chahal, Surinder Pall. Organophosphorus acids for hydrometallurgical extraction: The synthesis of --- phosphinic and --- phosphoric acids and their evaluation as potential hydrometallurgical extractants for cobalt or nickel.. Bradford, 1987.

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