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https://doi.org/10.1039/b603882d
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Cite Journal: Chem. Commun. |  Publication Date: Jan 1, 2006 |
 Citations: 17 |
Affiliation: Kyoto Institute of Technology
The Reformatsky-type reaction of 2-bromo-3,3,3-trifluoropropanoic imide with various types of imines, in the presence of ZnBr2 as a Lewis acid in THF at 0 degrees C for 3 h, gave the corresponding alpha-trifluoromethyl-beta-amino acid derivatives in a highly anti-selective manner.
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