Fig. 2: Reaction optimization studiesa. | Nature Communications

Fig. 2: Reaction optimization studiesa.

From: Skeletal editing of pyridines to aryldialdehydes

Fig. 2

A N-Activating group screening; B Secondary amine evaluation; C Reaction condition optimization; D Investigation into one-pot reactions. aYield was determined by 1H NMR using 1,2-dichloroethane as the internal standard; breaction conditions: 3-phenylpyridinium salt (0.1 mmol), pyrrolidine (0.2 mmol), (COCl)2 (10.0 equiv.), DMF (1.0 mL), CHCl3 (1.0 mL), 60 °C, 10 h; cN-DNP 3-phenylpyridinium salt (0.1 mmol), HNR2 (0.2 mmol) were used. dpyrrolidine (0.02 mmol, 0.2 equiv.) was used; CHCl3 = chloroform, DMF = N, N-Dimethylformamide.

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