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. Author manuscript; available in PMC: 2014 Aug 15.
Published in final edited form as: J Am Chem Soc. 2013 Aug 1;135(32):11799–11802. doi: 10.1021/ja407277a

Table 2.

Gram-scale substrate scope of Mannich reaction.a

graphic file with name nihms512233f4.jpg
a

Yields based on purified products. Diastereomeric ratios (dr) and enantiomeric excesses (ee) were determined by HPLC.

b

Yield determined by 1H NMR versus Bn2O as a standard; product characterized after hydrolysis of the benzophenone imine.

c

Reaction performed at a concentration of 0.07 M.

d

20 mol% catalyst was used; 0.9 mmol scale.