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. 2024 Oct 25;15:9227. doi: 10.1038/s41467-024-53605-7

Fig. 3. Scope of asymmetric Büchner reaction of N-propargyl ynamides 1.

Fig. 3

Reaction conditions: 1 (0.1 mmol), Cu(MeCN)4PF6 (0.01 mmol), L9 (0.012 mmol), NaBArF4 (0.012 mmol), toluene (2 mL), −20 °C, in vials; yields are those for the isolated products; ees are determined by HPLC analysis. aDCM (2 mL), 20 °C; bDCM (2 mL), 30 °C. Ts = p-toluenesulfonyl, Mbs = 4-methoxybenzenesulfonyl, Mts = 2-mesitylenesulfonyl, Bs = 4-bromobenzenesulfonyl, PMP = 4-methoxyphenyl.