Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/106879
Title: Copper-catalyzed enantioselective conjugate addition of grignard reagents to methyl 4,4,4-trifluorocrotonate : synthesis of enantioenriched trifluoromethylated compounds
Authors: Zhang, Li-Ying
Zhou, Jia-Hui
Xu, Yun-He
Loh, Teck-Peng
Keywords: DRNTU::Science::Chemistry::Organic chemistry::Carbanions
Issue Date: 2015
Source: Zhang, L.-Y., Zhou, J.-H., Xu, Y.-H., & Loh, T.-P. (2015). Copper-catalyzed enantioselective conjugate addition of grignard reagents to methyl 4,4,4-trifluorocrotonate : synthesis of enantioenriched trifluoromethylated compounds. Chemistry - an Asian journal, 10(4), 844-848.
Series/Report no.: Chemistry - an Asian journal
Abstract: Copper-catalyzed enantioselective 1,4-conjugate addition of methyl 4,4,4-trifluorocrotonate with aliphatic Grignard reagents to access an asymmetric tertiary carbon center attached with a trifluoromethyl group was achieved under mild reaction conditions. The desired products could be obtained in reasonable yields and good enantioselectivities.
URI: https://hdl.handle.net/10356/106879
http://hdl.handle.net/10220/25142
ISSN: 1861-4728
DOI: 10.1002/asia.201403303
Schools: School of Physical and Mathematical Sciences 
Rights: © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

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