User:Tsang Karl/Ketone Halogenation/Bibliography

== Bibliography ==

This is where you will compile the bibliography for your Wikipedia assignment. Add the name and/or notes about what each source covers, then use the "Cite" button to generate the citation for that source.


 * K. E. Teo, E. W. Warnhoff (1973). ".alpha.-Halo ketones. VII. Origin of disubstitution products in ketone halogenation. New mechanism" Journal of the American Chemical Society
 * This is a peer-review scientific journal, so it should be a reliable source. It goes into details of the origin of this process
 * Example: Roman, Bart I.; Kimpe, Norbert De; Stevens, Christian V. (2010-10-13). "Synthesis of β-, γ-, δ-, ..., ω-Halogenated Ketones and Aldehydes"
 * This is a journal article I pulled off the ACS website
 * Indicates different methods of halogenation without numerous types of positions besides the alpha position. Should expand on the halogenation of ketone since the article only covers what happens at the alpha position.
 * Pravst, Igor; Zupan, Marko; Stavber, Stojan (2008-05-26). "Halogenation of ketones with N-halosuccinimides under solvent-free reaction conditions". Tetrahedron. 64 (22): 5191–5199. doi:10.1016/j.tet.2008.03.048. ISSN 0040-4020.
 * This is a peer-review scientific journal, so it should be a reliable source
 * Looks into solvent free reaction in the hope of creating a green process

Papers to Read: Vražič, D., Jereb, M., Laali, K., &#38; Stavber, S. (2012). Brønsted Acidic Ionic Liquid Accelerated Halogenation of Organic Compounds with N-Halosuccinimides (NXS). Molecules, 18(1), 74–96. https://doi.org/10.3390/molecules18010074

Meshram, H. M., Reddy, P. N., Vishnu, P., Sadashiv, K., &#38; Yadav, J. S. (2006). A green approach for efficient α-halogenation of β-dicarbonyl compounds and cyclic ketones using N-halosuccinimides in ionic liquids. Tetrahedron Letters, 47(6), 991–995. https://doi.org/10.1016/j.tetlet.2005.11.141

Lao, Z., Zhang, H., &#38; Toy, P. H. (2019). Reductive Halogenation Reactions: Selective Synthesis of Unsymmetrical α-Haloketones. Organic Letters, 21(20), 8149–8152. https://doi.org/10.1021/acs.orglett.9b02324

Quintiliano, S. A. P., &#38; Silva Jr., L. F. (2007). A mild procedure for &#38;lt;FONT FACE=Symbol&#38;gt;a,a&#38;lt;/FONT&#38;gt;-dichlorination of cyclic aryl ketones using commercial bleach. Journal of the Brazilian Chemical Society, 18(6), 1281–1284. https://doi.org/10.1590/S0103-50532007000600026

Wang, Z., Yin, G., Qin, J., Gao, M., Cao, L., &#38; Wu, A. (2008). An Efficient Method for the Selective Iodination of α,β-Unsaturated Ketones. Synthesis, 2008(22), 3675–3681. https://doi.org/10.1055/s-0028-1083200

le Bras, G., Provot, O., Bekaert, A., Peyrat, J.-F., Alami, M., &#38; Brion, J.-D. (2006). α-Iodination of Ketones with MnO 2 /I 2 Reagent Combination: A New Environmentally Friendly Procedure. Synthesis, 2006(9), 1537–1541. https://doi.org/10.1055/s-2006-926435

Sreedhar, B., Surendra Reddy, P., &#38; Madhavi, M. (2007). Rapid and Catalyst‐Free α‐Halogenation of Ketones using N ‐Halosuccinamides in DMSO. Synthetic Communications, 37(23), 4149–4156. https://doi.org/10.1080/00397910701574908