Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/100554
Title: Application of recyclable ionic liquid-supported imidazolidinone catalyst in enantioselective Diels–Alder reactions
Authors: Shen, Zhi-Liang
Cheong, Hao-Lun
Lai, Yin-Chang
Loo, Wan-Yi
Loh, Teck-Peng
Issue Date: 2012
Source: Shen, Z.-L., Cheong, H.-L., Lai, Y.-C., Loo, W.-Y., & Loh, T.-P. (2012). Application of recyclable ionic liquid-supported imidazolidinone catalyst in enantioselective Diels–Alder reactions. Green Chemistry, 14(9), 2626-2630.
Series/Report no.: Green chemistry
Abstract: The application of ionic liquid-supported imidazolidinone catalyst I in enantioselective Diels–Alder reactions was investigated. The Diels–Alder reactions involving α,β-unsaturated aldehydes and cyclopentadiene proceeded efficiently in the presence of catalyst I to provide the desired products in moderate to good yields with good to excellent enantioselectivities. Especially noteworthy, catalyst I can be recovered and reused for up to five runs while maintaining its high catalytic activity.
URI: https://hdl.handle.net/10356/100554
http://hdl.handle.net/10220/16292
DOI: http://dx.doi.org/10.1039/c2gc35966a
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

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