Copper-catalyzed enantioselective conjugate addition of grignard reagents to methyl 4,4,4-trifluorocrotonate : synthesis of enantioenriched trifluoromethylated compounds
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 rea...
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sg-ntu-dr.10356-1068792019-12-06T22:20:12Z Copper-catalyzed enantioselective conjugate addition of grignard reagents to methyl 4,4,4-trifluorocrotonate : synthesis of enantioenriched trifluoromethylated compounds Zhang, Li-Ying Zhou, Jia-Hui Xu, Yun-He Loh, Teck-Peng School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Organic chemistry::Carbanions 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. 2015-03-02T06:56:38Z 2019-12-06T22:20:12Z 2015-03-02T06:56:38Z 2019-12-06T22:20:12Z 2015 2015 Journal Article 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. 1861-4728 https://hdl.handle.net/10356/106879 http://hdl.handle.net/10220/25142 http://dx.doi.org/10.1002/asia.201403303 en Chemistry - an Asian journal © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
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DRNTU::Science::Chemistry::Organic chemistry::Carbanions Zhang, Li-Ying Zhou, Jia-Hui Xu, Yun-He Loh, Teck-Peng Copper-catalyzed enantioselective conjugate addition of grignard reagents to methyl 4,4,4-trifluorocrotonate : synthesis of enantioenriched trifluoromethylated compounds |
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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. |
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School of Physical and Mathematical Sciences |
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School of Physical and Mathematical Sciences Zhang, Li-Ying Zhou, Jia-Hui Xu, Yun-He Loh, Teck-Peng |
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Article |
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Zhang, Li-Ying Zhou, Jia-Hui Xu, Yun-He Loh, Teck-Peng |
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Zhang, Li-Ying |
title |
Copper-catalyzed enantioselective conjugate addition of grignard reagents to methyl 4,4,4-trifluorocrotonate : synthesis of enantioenriched trifluoromethylated compounds |
title_short |
Copper-catalyzed enantioselective conjugate addition of grignard reagents to methyl 4,4,4-trifluorocrotonate : synthesis of enantioenriched trifluoromethylated compounds |
title_full |
Copper-catalyzed enantioselective conjugate addition of grignard reagents to methyl 4,4,4-trifluorocrotonate : synthesis of enantioenriched trifluoromethylated compounds |
title_fullStr |
Copper-catalyzed enantioselective conjugate addition of grignard reagents to methyl 4,4,4-trifluorocrotonate : synthesis of enantioenriched trifluoromethylated compounds |
title_full_unstemmed |
Copper-catalyzed enantioselective conjugate addition of grignard reagents to methyl 4,4,4-trifluorocrotonate : synthesis of enantioenriched trifluoromethylated compounds |
title_sort |
copper-catalyzed enantioselective conjugate addition of grignard reagents to methyl 4,4,4-trifluorocrotonate : synthesis of enantioenriched trifluoromethylated compounds |
publishDate |
2015 |
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https://hdl.handle.net/10356/106879 http://hdl.handle.net/10220/25142 http://dx.doi.org/10.1002/asia.201403303 |
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1681044433322115072 |