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1

Palmer, David C., ed. Oxazoles: Synthesis, Reactions, and Spectroscopy. John Wiley & Sons, Inc., 2004. http://dx.doi.org/10.1002/0471649295.

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2

Trethewey, Andrew Nicholas. Synthesis and evaluation of perhydro-oxazolo [3,4-a] pyridines as fungicides. Portsmouth Polytechnic, 1985.

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3

Palmer, David C., ed. Oxazoles: Synthesis, Reactions, and Spectroscopy, Part A. John Wiley & Sons, Inc., 2003. http://dx.doi.org/10.1002/0471428035.

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4

Grünanger, Paolo. Isoxazoles. Wiley, 1991.

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5

Jones, Gary B. Design, synthesis and evaluation of DNA-binding oxazolo[2,3-c][1,4] benzodiazepines and pyrrolo[2,1-c][1,4] benzodiazepines. Portsmouth Polytechnic, School of Pharmacy and Biomedical Sciences, 1991.

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6

1957-, Kumar M., and Gupta V. 1966-, eds. Heterocyclic chemistry. Springer, 1998.

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7

Turchi, I. J. Oxazoles. Wiley & Sons, Incorporated, John, 2009.

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8

J, Turchi I., ed. Oxazoles. Wiley, 1986.

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9

Palmer, David C. Oxazoles: Synthesis, Reactions, and Spectroscopy, Part A. Wiley & Sons, Incorporated, John, 2008.

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10

C, Palmer David, ed. Oxazoles: Synthesis, reactions, and spectroscopy. Wiley, 2003.

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11

Palmer, David C. Oxazoles: Synthesis, Reactions, and Spectroscopy, Part B. Wiley & Sons, Incorporated, John, 2004.

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12

Palmer, David C. Oxazoles: Synthesis, Reactions, and Spectroscopy, Part A. Wiley & Sons, Incorporated, John, 2003.

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13

Doyle, Kevin James. Rhodium carbenoid route to oxazoles. 1994.

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14

Oxazoles: Synthesis, reactions, and spectroscopy. Wiley, 2003.

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15

United States. Environmental Protection Agency. Prevention, Pesticides, and Toxic Substances., ed. Interim reregistration eligibility decision (IRED): Oxamyl. U.S. Environmental Protection Agency, Prevention, Pesticides and Toxic Substances, 2000.

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16

United States. Environmental Protection Agency. Prevention, Pesticides, and Toxic Substances., ed. Interim reregistration eligibility decision (IRED): Oxamyl. U.S. Environmental Protection Agency, Prevention, Pesticides and Toxic Substances, 2000.

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17

Turchi, I. J. The Chemistry of Heterocyclic Compounds, Oxazoles. Wiley-Interscience, 1986.

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18

United States. Environmental Protection Agency. Prevention, Pesticides, and Toxic Substances., ed. Interim reregistration eligibility decision (IRED): Oxamyl. U.S. Environmental Protection Agency, Prevention, Pesticides and Toxic Substances, 2000.

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19

(Editor), Paola Grünanger, Paola Vita-Finzi (Editor), and James E. Dowling (Editor), eds. The Chemistry of Heterocyclic Compounds, Isoxazoles (Chemistry of Heterocyclic Compounds: A Series Of Monographs). Wiley-Interscience, 1999.

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20

Grünanger, Paola, and Paola Vita-Finzi. Volume 49, Part 1, Isoxazoles. Wiley-Interscience, 1991.

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21

Palmer, David C. The Chemistry of Heterocyclic Compounds, Oxazoles: Synthesis, Reactions, and Spectroscopy, Part A. Wiley-Interscience, 2003.

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22

Palmer, David C. The Chemistry of Heterocyclic Compounds, Oxazoles: Synthesis, Reactions, and Spectroscopy, Part B. Wiley-Interscience, 2004.

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23

Palmer, David C. The Chemistry of Heterocyclic Compounds, Oxazoles: Synthesis, Reactions, and Spectroscopy, Parts A & B. Wiley-Interscience, 2004.

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24

Roy, Amelie. Synthetic studies of the formation of oxazoles and isoxazoles from N-acetoacetyl derivatives: Scope and limitations AND Aqueous rhodium-catalyzed Heck-type coupling reactions between boronic acids and olefins. 2000.

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25

Gupta, Radha R., Vandana Gupta, and Mahendra Kumar. Heterocyclic Chemistry II: Five-Membered Heterocycles (Heterocyclic Chemistry). Springer, 1999.

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