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. 2018 Jul 19;9:2841. doi: 10.1038/s41467-018-05192-7

Fig. 2.

Fig. 2

Synthesis of α-amino amides. a Scope with respect to the tertiary amide. b Scope with respect to the isocyanide. Standard condition: amide 0.3 mmol, IrCl(CO)(PPh3)2 1 mol%, TMDS 0.6 mmol, CH2Cl2 3 mL, isocyanide 0.6 mmol, CH3COOH 0.36 mmol; yields of purified product following flash column chromatography; areaction was performed at 50 °C after the addition of tert-butyl isocyanide and CH3COOH; bwith 0.9 mmol CH3COOH