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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Main Author: Choo, En
Other Authors: Loh Teck Peng
Format: Theses and Dissertations
Published: 2011
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Online Access:http://hdl.handle.net/10356/47514
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Institution: Nanyang Technological University
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spelling 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
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
topic DRNTU::Science::Chemistry::Organic chemistry::Organic synthesis
spellingShingle 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
description 118 p.
author2 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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