Fig. 3 | Nature Communications

Fig. 3

From: Enantiodivergence by minimal modification of an acyclic chiral secondary aminocatalyst

Fig. 3The alternative text for this image may have been generated using AI.

Mannich reaction of trifluoromethyl alkynyl ketimines. Reaction conditions for the formation of (S,R)-5: 4 (0.1 mmol), PNBA (0.02 mmol, 20 mol %), Ia/0.5TfOH (20 mol %), 2 (0.3 mmol), MeCN (0.8 mL), −20 °C. Reaction conditions for the formation of (R,S)-5: 4 (0.1 mmol), PNBA (0.02 mmol, 20 mol %), Id/0.5TfOH (20 mol %), 2 (0.3 mmol), MeOH (0.8 mL), −20 °C. Single asterisk (*): Without PNBA as the additive. Double asterisks (**): Without PNBA as the additive. MeCN as the solvent (The absolute and relative configuration of 5k was determined by comparison with the reported ref. 50.)

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