2010
DOI: 10.1002/chin.201039193
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ChemInform Abstract: Enantioselective Synthesis of β‐Trifluoromethyl α‐Amino Acids.

Abstract: Enantioselective Synthesis of β-Trifluoromethyl α-Amino Acids. -The structure of the chiral catalysts is essential for the enantioselective hydrogenation of either (Z)-alkyl or (Z)-aryl trifluoroamidoenoates. Enantiopure trifluorovalin is obtained from (IIa). Other selective deprotection reactions of (IIa) are demonstrated. -(BENHAIM*, C.; BOUCHARD, L.; PELLETIER, G.; SELLSTEDT, J.; KRISTOFOVA, L.; DAIGNEAULT, S.; Org. Lett. ; Wyeth Res., St-Laurent, Que. H4R 1J6, Can.; Eng.) -R. Steudel 39-193 s

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