Synthesis and application of a recyclable ionic liquid-supported imidazolidinone catalyst in enantioselective 1,3-dipolar cycloaddition

The synthesis of recyclable ionic liquid-supported imidazolidinone catalyst I and its application in 1,3-dipolar cycloaddition of nitrone with α,β-unsaturated aldehyde with high performance were described. Most importantly, the catalyst I can be recovered and recycled for up to five runs without obs...

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Main Authors: Yang, Yong Sheng, Shen, Zhi-Liang, Goh, Kau Kiat Kelvin, Wong, Colin Hong An, Loo, Wan-Yi, Lu, Jun, Loh, Teck-Peng
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/101358
http://hdl.handle.net/10220/11124
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1013582020-03-07T12:34:43Z Synthesis and application of a recyclable ionic liquid-supported imidazolidinone catalyst in enantioselective 1,3-dipolar cycloaddition Yang, Yong Sheng Shen, Zhi-Liang Goh, Kau Kiat Kelvin Wong, Colin Hong An Loo, Wan-Yi Lu, Jun Loh, Teck-Peng School of Physical and Mathematical Sciences The synthesis of recyclable ionic liquid-supported imidazolidinone catalyst I and its application in 1,3-dipolar cycloaddition of nitrone with α,β-unsaturated aldehyde with high performance were described. Most importantly, the catalyst I can be recovered and recycled for up to five runs without observing significant decrease in catalytic activity. 2013-07-10T07:35:17Z 2019-12-06T20:37:08Z 2013-07-10T07:35:17Z 2019-12-06T20:37:08Z 2012 2012 Journal Article Shen, Z.-L., Goh, K. K. K., Wong, C. H. A., Loo, W.-Y., Yang, Y.-S., Lu, J., et al. (2012). Synthesis and application of a recyclable ionic liquid-supported imidazolidinone catalyst in enantioselective 1,3-dipolar cycloaddition. Chemical Communications, 48(47), 5856-5858. https://hdl.handle.net/10356/101358 http://hdl.handle.net/10220/11124 10.1039/c2cc31830j en Chemical communications © 2012 The Royal Society of Chemistry.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
description The synthesis of recyclable ionic liquid-supported imidazolidinone catalyst I and its application in 1,3-dipolar cycloaddition of nitrone with α,β-unsaturated aldehyde with high performance were described. Most importantly, the catalyst I can be recovered and recycled for up to five runs without observing significant decrease in catalytic activity.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Yang, Yong Sheng
Shen, Zhi-Liang
Goh, Kau Kiat Kelvin
Wong, Colin Hong An
Loo, Wan-Yi
Lu, Jun
Loh, Teck-Peng
format Article
author Yang, Yong Sheng
Shen, Zhi-Liang
Goh, Kau Kiat Kelvin
Wong, Colin Hong An
Loo, Wan-Yi
Lu, Jun
Loh, Teck-Peng
spellingShingle Yang, Yong Sheng
Shen, Zhi-Liang
Goh, Kau Kiat Kelvin
Wong, Colin Hong An
Loo, Wan-Yi
Lu, Jun
Loh, Teck-Peng
Synthesis and application of a recyclable ionic liquid-supported imidazolidinone catalyst in enantioselective 1,3-dipolar cycloaddition
author_sort Yang, Yong Sheng
title Synthesis and application of a recyclable ionic liquid-supported imidazolidinone catalyst in enantioselective 1,3-dipolar cycloaddition
title_short Synthesis and application of a recyclable ionic liquid-supported imidazolidinone catalyst in enantioselective 1,3-dipolar cycloaddition
title_full Synthesis and application of a recyclable ionic liquid-supported imidazolidinone catalyst in enantioselective 1,3-dipolar cycloaddition
title_fullStr Synthesis and application of a recyclable ionic liquid-supported imidazolidinone catalyst in enantioselective 1,3-dipolar cycloaddition
title_full_unstemmed Synthesis and application of a recyclable ionic liquid-supported imidazolidinone catalyst in enantioselective 1,3-dipolar cycloaddition
title_sort synthesis and application of a recyclable ionic liquid-supported imidazolidinone catalyst in enantioselective 1,3-dipolar cycloaddition
publishDate 2013
url https://hdl.handle.net/10356/101358
http://hdl.handle.net/10220/11124
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