Skip to main content
. Author manuscript; available in PMC: 2019 Jan 25.
Published in final edited form as: J Am Chem Soc. 2013 Oct 15;135(42):15742–15745. doi: 10.1021/ja409241h

Table 2.

Scope of (MeObpy)CuI/ABNO-Catalyzed Aerobic Secondary Alcohol Oxidationa

graphic file with name nihms-1005005-t0008.jpg
a

Yields given are for isolated material. All reactions were performed on a 1 mmol scale in 10 mL of MeCN for 1 h in an open reaction vessel, unless otherwise noted.

b

>99% ee. 0.75 h reaction time.

c

Benzoin used as starting material.

d

Reaction performed at 70 °C with O2 balloon.10

e

2 h reaction time; 2 mol % catalyst added after 1.5 h (see SI for details).

f

1H NMR yield.

g

Isolated as the 2,4-dinitrophenylhydrazone due to product volatility.

h

Isolated as the HCl salt.

i

Reaction performed at 60 °C.10

j

0.5 reaction time.

k

0.2 M substrate concentration.