Part I: Development of a base-free methodology for the nh-catalyzed intermolecular stetter reaction. Part II: Chiral anion mediated asymmetric stetter reaction
118 p.
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2011
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sg-ntu-dr.10356-475142023-02-28T23:46:52Z Part I: Development of a base-free methodology for the nh-catalyzed intermolecular stetter reaction. Part II: Chiral anion mediated asymmetric stetter reaction Choo, En Loh Teck Peng School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Organic chemistry::Organic synthesis 118 p. We succeeded in developing a base-free methodology for the NHC-catalyzed intermolecular Stetter reaction by employing CsF as a dual Lewis acid/base activating reagent, achieving the desired 1,4-dicarbonyl structural scaffold under ultrasonication reaction condition. Generally, moderate to excellent yields were obtained. Yields were especially good when highly reactive Michael acceptors were employed in conjuction with an aromatic carbinol carrying electron withrdrawing subtituents. Master of Science 2011-12-27T08:31:55Z 2011-12-27T08:31:55Z 2009 2009 Thesis http://hdl.handle.net/10356/47514 Nanyang Technological University application/pdf |
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DRNTU::Science::Chemistry::Organic chemistry::Organic synthesis Choo, En Part I: Development of a base-free methodology for the nh-catalyzed intermolecular stetter reaction. Part II: Chiral anion mediated asymmetric stetter reaction |
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118 p. |
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Loh Teck Peng |
author_facet |
Loh Teck Peng Choo, En |
format |
Theses and Dissertations |
author |
Choo, En |
author_sort |
Choo, En |
title |
Part I: Development of a base-free methodology for the nh-catalyzed intermolecular stetter reaction. Part II: Chiral anion mediated asymmetric stetter reaction |
title_short |
Part I: Development of a base-free methodology for the nh-catalyzed intermolecular stetter reaction. Part II: Chiral anion mediated asymmetric stetter reaction |
title_full |
Part I: Development of a base-free methodology for the nh-catalyzed intermolecular stetter reaction. Part II: Chiral anion mediated asymmetric stetter reaction |
title_fullStr |
Part I: Development of a base-free methodology for the nh-catalyzed intermolecular stetter reaction. Part II: Chiral anion mediated asymmetric stetter reaction |
title_full_unstemmed |
Part I: Development of a base-free methodology for the nh-catalyzed intermolecular stetter reaction. Part II: Chiral anion mediated asymmetric stetter reaction |
title_sort |
part i: development of a base-free methodology for the nh-catalyzed intermolecular stetter reaction. part ii: chiral anion mediated asymmetric stetter reaction |
publishDate |
2011 |
url |
http://hdl.handle.net/10356/47514 |
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1759855788042485760 |