An eco-friendly and very low catalyst loading continuous condensation of primary amines and 1,3 Di carbonyl compounds: Synthesis of enaminones and enaminoesters by microreactor technology
Author:
Funder
University of Isfahan
Publisher
Springer Science and Business Media LLC
Subject
Organic Chemistry,Fluid Flow and Transfer Processes,Chemistry (miscellaneous)
Link
https://link.springer.com/content/pdf/10.1007/s41981-023-00263-3.pdf
Reference68 articles.
1. Elassar AZA, El-Khair AA (2003) Recent developments in the chemistry of enaminones. Tetrahedron 59:8463–8480. https://doi.org/10.1016/S0040-4020(03)01201-8
2. Wan JP, Cao S, Liu Y (2016) Base-Promoted Synthesis of N-Substituted 1,2,3-Triazoles via Enaminone-Azide Cycloaddition Involving Regitz Diazo Transfer. Org Lett 18:6034–6037. https://doi.org/10.1021/acs.orglett.6b02975
3. Chen G, Wang Z, Zhang X, Fan X (2017) Synthesis of Functionalized Pyridines via Cu(II)-Catalyzed One-Pot Cascade Reactions of Inactivated Saturated Ketones with Electron-Deficient Enamines. J Org Chem 82:11230–11237. https://doi.org/10.1021/acs.joc.7b01901
4. Alexander MS, Scott KR, Harkless J et al (2013) Enaminones 11. An examination of some ethyl ester enaminone derivatives as anticonvulsant agents. Bioorganic Med Chem 21:3272–3279. https://doi.org/10.1016/j.bmc.2013.03.036
5. Wu W, Wang Z, Shen Q et al (2019) Fe-Catalyzed enaminone synthesis from ketones and amines. Org Biomol Chem 17:6753–6756. https://doi.org/10.1039/c9ob01137d
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