User:Elbert Ainsteinium/Michael reaction/Bibliography

List of sources for Wikipedia assignment

 * Brown, W.H., Iverson, B.L., Anslyn, & E., Foote, C.S. (2018). Organic Chemistry, 8th Edition. Cengage Learning. ISBN: 978-1-305-58035-0
 * This was our CHEM 203/213 textbook, so it should be reliable and provide a suitable base-line understanding of the Michael reaction
 * Note: automatic citation needs to be checked
 * Krishna, P.R., Sreeshailam, A., & Srinivas, R. (2009). Recent advances and applications in asymmetric aza-Michael addition chemistry. 65(47), 9657-9672. 10.1016/j.tet.2009.08.021
 * This review article has been published under a well-known journal (Elsevier) so it should be a reliable source. It details the use of aza-Michael additions, and can be used to provide further detail on that subsection of the Michael reaction
 * There is no declaration related to conflict of interest
 * Note: automatic citation needs to be checked
 * Vinogradov, M.G., Turova, O.V., & Zlotin, S.G. (2019). Recent advances in the asymmetric synthesis of pharmacology-relevant nitrogen heterocycles via stereoselective aza-Michael reactions. 76(28-29), 3670-3708. 10.1039/c8ob03034k
 * This review article has been published under a peer-reviewed journal (Organic and Biomolecular Chemistry), so it should be a reliable source. It provides a more recent review (compared to the second citation in this list) of stereoselective aza-Michael reactions. This review can be used to search retroactively search for examples of aza-Michael reactions.
 * The sources in this review article can be compared to the sources in the other review article (the second citation in this list) to evaluate the extent of information regarding aza-Michael reactions
 * The authors declare no conflict of interest.
 * Note: automatic citation needs to be checked, for the volume and issue numbers don't appear to be correct
 * Wada, Makoto; Takeichi, Eiji; Matsumoto, Takashi (1991-03-01). "Bismuth Trichloride as a New Efficient Catalyst in the Aldol Reaction and the Michael Reaction". Bulletin of the Chemical Society of Japan. 64 (3): 990–994. 10.1246/bcsj.64.990
 * Published in Bulletin of the Chemical Society of Japan by The Chemical Society of Japan
 * Talks about catalytic Micheal addition using Bismuth Trichloride catalyst
 * Ahadi, S.; Naghdiani, Z.; Balalaie, S.; Rominger, F. (2015-09-23). "Diastereoselective synthesis of polysubstituted cyclopentanols and cyclopentenes containing stereogenic centers via domino Michael/cyclization reaction". Tetrahedron. 71 (38): 6860–6866. 10.1016/j.tet.2015.07.022.
 * Published in Tetrahedron by Elsevier
 * Talks about stereoselective Micheal addition


 * Chauhan, P.; Kaya, U.; Enders, D. Advances in Organocatalytic 1,6-Addition Reactions: Enantioselective Construction of Remote Stereogenic Centers. Adv. Synth. Catal. 2017, 359 (6), 888-912. DOI: 10.1002/adsc.20160134.
 * Published in Advanced Synthesis and Catalysis
 * Review article (secondary source) discussing 1,6-Michael additions
 * Note: automatic citation is not working, so need to manually enter


 * Choudhury, A.R.; Mukherjee, S. Deconjugated butenolide: a versatile building block for asymmetric catalysis. Chem. Soc. Rev. 2020, 49 (18), 6755-6788. DOI: 10.1039/c9cs00346k.
 * High journal impact factor
 * Only briefly talks about 1,6-Michael additions, so may not be super important. However, it's worth checking out.
 * Review article (secondary source)