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Bifunctional 2 aminoDMAP thiourea catalyzed enantioselective Michael addition of thioacetic acid to trans beta nitrostyrenes
Date
2016-03-24
Author
Tözendemir, Deniz
Tanyeli, Cihangir
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https://hdl.handle.net/11511/87264
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Bifunctional 2-aminodmap/thiourea catalyzed enantioselective michael addition of thioacetic acid to trans-beta-nitrostyrenes
Kabasakal, Zehra; Tanyeli, Cihangir; Department of Chemistry (2013)
Michael addition reactions as an efficient method for carbon-carbon bond formations have been intensively explored in the context of enantioselective organocatalysis using aldehydes, ketones, 1,3- dicarbonyl compounds and nitroalkenes as donors. However, there are very few studies using thiol derivative as a nucleophile. In this thesis, enantioselective Michael addition reaction of thioacetic acid as Michael donor and 10 trans-β-nitrostyrene derivatives as Michael acceptors have been studied. The products o...
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D. Tözendemir and C. Tanyeli, “Bifunctional 2 aminoDMAP thiourea catalyzed enantioselective Michael addition of thioacetic acid to trans beta nitrostyrenes,” 2016, Accessed: 00, 2021. [Online]. Available: https://hdl.handle.net/11511/87264.