Skip to main content
. Author manuscript; available in PMC: 2016 Jan 19.
Published in final edited form as: Angew Chem Int Ed Engl. 2014 Nov 25;54(4):1312–1315. doi: 10.1002/anie.201410322

Table 3.

Dehydrogenative cross-coupling of aldehydes and amines.[a]

graphic file with name nihms647078f6.jpg
[a]

Conditions: 0.5 mmol 1, 0.5 mmol 6, 0.2 M, 8 h. Isolated yields are shown.

[b]

The reactions were performed at 40 °C using IPr as the ligand and 3d as the hydrogen acceptor.

[c]

The reactions were performed at 30 °C using IPr as a ligand and 3d as the hydrogen acceptor.

[d]

The reactions were performed at 40 °C using ItBu as the ligand and an extra equivalent of the aldehyde as the hydride acceptor.

[e]

Using 1a rather than cyclohexanecarboxaldehyde as the hydrogen acceptor.