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1

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

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2

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

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3

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

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4

Hudlický, Miloš. Reductions in organic chemistry. 2nd ed. Washington, D.C: American Chemical Society, 1996.

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5

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

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6

Larson, G. L. Ionic and organometallic-catalyzed organosilane reductions. Hoboken, N.J: Wiley, 2010.

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7

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

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8

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

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9

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

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10

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

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11

Seyden-Penne, J. Reductions by the alumino- and borohydrides in organic synthesis. New York: 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. New York, N.Y: 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. Chichester [West Sussex]: 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. Weinheim: 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. Washington, DC: 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. Hoboken, N.J: 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. Weinheim, Federal Republic of Germany: 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. Chichester, West Sussex, England: 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 and oxidative metabolism, and in separate chapters discusses the oxidation-reduction thermodynamics of oxygen species, and the nature of the bonding for oxygen in its compounds. Additional chapters focus on the reactivities of specific oxygen compounds. The book will be of interest to chemists and biochemists, as well as graduate students, life scientists, and medical researchers.
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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 outlined are the introduction of fluorine into organic molecules, reduction and oxidation of fluorine compounds, reactions of fluorocompounds with halogens and their derivatives, nitration, acid catalyzed reactions, organometallic syntheses, and pyrolyses. The reactions are documented in the experimental material of the earlier volumes and will be important background knowledge for anyone working in organic chemistry.
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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 reactions, as it is an excellent solvent, being able to dissolve gases and many solids. Moreover, Atkins tells us that water is actually chemically aggressive, and can react with and destroy the compounds dissolved in it, and he shows us what happens at the molecular level when water turns to ice--and when it melts. Moving beyond water, Atkins slowly builds up a toolkit of basic chemical processes, including precipitation (perhaps the simplest of all chemical reactions), combustion, reduction, corrosion, electrolysis, and catalysis. He then shows how these fundamental tools can be brought together in more complex processes such as photosynthesis, radical polymerization, vision, enzyme control, and synthesis. Peter Atkins is the world-renowned author of numerous best-selling chemistry textbooks for students. In this crystal-clear, attractively illustrated, and insightful volume, he provides a fantastic introductory tour--in just a few hundred colorful and lively pages - for anyone with a passing or serious interest in chemistry.
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