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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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