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Books on the topic 'Nitro compounds. Reduction (Chemistry)'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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1

Cenini, Sergio. Catalytic reductive carbonylation of organic nitro compounds. Kluwer Academic Publishers, 1997.

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2

Hudlicky, Milos. Reductions in organic chemistry. 2nd ed. American Chemical Society, 1996.

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3

Oxidation and reduction in organic synthesis. Oxford University Press, 2000.

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4

Hudlický, Miloš. Reductions in organic chemistry. 2nd ed. American Chemical Society, 1996.

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5

Valentin, Lopyrev, ed. Nitroazoles: Synthesis, structure and applications. Springer, $c c2009., 2009.

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6

Larson, G. L. Ionic and organometallic-catalyzed organosilane reductions. Wiley, 2010.

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7

Mennekes, Theodor. Zur Reduktion von Dihalogenorganylboranen mit Alkalimetallen. Verlag Shaker, 1992.

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8

Penne, J. Seyden. Reductions by the alumino- and borohydrides in organic synthesis. VCH Verlagsgesellschaft, 1991.

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9

Lappin, Graham. Redox mechanisms in inorganic chemistry. Ellis Horwood, 1994.

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10

Reductions by the alumino- and borohydrides in organic synthesis. 2nd ed. Wiley-VCH, 1997.

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11

Seyden-Penne, J. Reductions by the alumino- and borohydrides in organic synthesis. VCH Publishers, 1991.

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12

Cenini, S., and F. Ragaini. Catalytic Reductive Carbonylation of Organic Nitro Compounds. Springer, 2010.

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13

Feuer, Henry, and Arnold T. Nielsen. Nitro Compounds: Recent Advances in Synthesis and Chemistry (Organic Nitro Chemistry). John Wiley & Sons, 1990.

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14

1912-, Feuer Henry, and Nielsen Arnold, eds. Nitro compounds: Recent advances in synthesis and chemistry. VCH, 1990.

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15

(Editor), Henry Feuer, and Arnold T. Nielson (Editor), eds. Nitro Compounds: Recent Advances in Synthesis and Chemistry. Vch Pub, 1990.

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16

Saul, Patai, ed. The chemistry of amino, nitroso, nitro, and related groups. Wiley, 1996.

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17

(Editor), H. Feuer, and A. T. Nielsen (Editor), eds. Recent Developments in the Synthesis and Chemistry of Nitro Compounds. Wiley-VCH, 1990.

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18

Patai, Saul. Part 2, The Chemistry of Amino, Nitroso, Nitro and Related Groups, Supplement F2. Wiley, 1996.

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19

(Editor), Pher Andersson, and Ian Munslow (Editor), eds. Modern Reduction Methods. Wiley-VCH, 2008.

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20

1963-, Andersson Pher G., and Munslow Ian J, eds. Modern reduction methods. Wiley-VCH, 2008.

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21

Andersson, Pher G., and Ian J. Munslow. Modern Reduction Methods. Wiley & Sons, Incorporated, John, 2008.

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22

Andersson, Pher G., and Ian J. Munslow. Modern Reduction Methods. Wiley & Sons, Limited, John, 2008.

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23

Nitrile Oxides, Nitrones & Nitronates in Organic Synthesis: Novel Strategies in Synthesis (Organic Nitro Chemistry). 2nd ed. Wiley, 2008.

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24

Larina, Lyudmila, and Valentin Lopyrev. Nitroazoles: Synthesis, Structure and Applications. Springer, 2010.

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25

Nitroazoles: Synthesis, Structure and Applications. Springer, 2012.

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26

Broderick, William E. Synthetic utility of Chromium (II)/(III) and Cobalt (II)/(III) redox chemistry mediated by coordinated ligands. 1986.

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27

1947-, Abdel-Magid Ahmed F., American Chemical Society. Division of Organic Chemistry., and American Chemical Society Meeting, eds. Reductions in organic synthesis: Recent advances and practical applications. American Chemical Society, 1996.

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28

Roberts, Stanley M., and John Whittall. Regio- and Stereo-Controlled Oxidations and Reductions. Wiley & Sons, Incorporated, John, 2007.

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29

Cozza, Cynthia L. A model for the prediction of biologically mediated reductive dechlorination pathways. 1990.

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30

Borchardt, Daniel Bryan. Electron transfer studies on some cobalt clathrochelates in nonaqueous solution. 1985.

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31

M, Roberts Stanley, and Whittall John, eds. Regio- and stereo-controlled oxidations and reductions. John Wiley, 2007.

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32

(Editor), Stanley M. Roberts, and John Whittall (Editor), eds. Catalysts for Fine Chemical Synthesis, Regio- and Stereo-Controlled Oxidations and Reductions (Catalysts For Fine Chemicals Synthesis). Wiley-Interscience, 2007.

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33

W, Gorrod J., and Damani L. A. 1949-, eds. Biological oxidation of nitrogen in organic molecules: Chemistry, toxicology, and pharmacology. VCH, 1985.

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34

Laughlin, James B. Investigation of the oxidation of small biochemical compounds entrapped in porous solids prepared by a sol-gel process. 1999.

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35

M, Roberts Stanley, and Poignant Geraldine, eds. Hydrolysis, oxidation and reduction. Wiley, 2002.

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36

Abdel-Magid, Ahmed F. Reductions in Organic Synthesis: Recent Advances and Practical Applications (Acs Symposium Series). An American Chemical Society Publication, 1998.

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37

Sawyer, Donald T., and R. J. P. Williams. Oxygen Chemistry. Oxford University Press, 1992. http://dx.doi.org/10.1093/oso/9780195057980.001.0001.

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This book places oxygen on the center stage of chemistry in a manner that parallels the focus on carbon by 19th century chemists. One measure of the significance of oxygen chemistry is the greater diversity of oxygen-containing molecules than of carbon-containing molecules. One of the most important compounds is water, containing the properties of being a unique medium for biological chemistry and life, the source of all the dioxygen in the atmosphere, and the moderator of the earth's climate. Sawyer first introduces the biological origins of dioxygen and role of dioxygen in aerobic biology an

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38

Hudlic'ky, Milos. Fluorine Chemistry for Organic Chemists. Oxford University Press, 2000. http://dx.doi.org/10.1093/oso/9780195131567.001.0001.

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This book is a synthesis of two of Hudlicky's earlier books outlining the many unpredictable properties of fluorine and its compounds that are not analogous to the properties of any other halogens and their compounds. It is divided into two separate sections, the first presenting peculiar reactions as problems to be solved. Each reaction can be analyzed in the lab without the help of the second section, however if a solution is not easily reached, the second section provides discussion of the problems, outlining the products of the reactions and their mechanisms. Among the 105 reactions outlin

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39

Promises and Limits of Reductionism in the Biomedical Sciences (Catalysts for Fine Chemical Synthesis). Wiley, 2002.

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40

Atkins, Peter. Reactions. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199695126.001.0001.

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Illustrated with remarkable new full-color images--indeed, one or more on every page--and written by one of the world's leading authorities on the subject, Reactions offers a compact, pain-free tour of the inner workings of chemistry. Reactions begins with the chemical formula almost everyone knows--the formula for water, H2O--a molecule with an "almost laughably simple chemical composition." But Atkins shows that water is also rather miraculous--it is the only substance whose solid form is less dense than its liquid (hence ice floats in water)--and incredibly central to many chemical reaction

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