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. Author manuscript; available in PMC: 2012 Feb 1.
Published in final edited form as: Chem Sci. 2012;3(1):58–61. doi: 10.1039/c1sc00556a

Table 2.

Enantioselective formyl α-oxidation: aldehyde scope

graphic file with name nihms348260f2.jpg
a

Isolated yields of aldehyde product (1.0 mmol scale).

b

Enantiomeric excess determined by chiral HPLC on corresponding alcohol or m-nitrobenzoyl ester.

c

Performed at −40 °C.

d

Ethyl acetate as solvent.