Skip to main content
. Author manuscript; available in PMC: 2014 Jul 10.
Published in final edited form as: Tetrahedron Lett. 2013 Jul 10;54(28):3627–3629. doi: 10.1016/j.tetlet.2013.04.116

Table 1.

Chrial γ-fluoroamines 10a–g via organocatalysis

graphic file with name nihms-479823-t0008.jpg

Starting material Yield of 9a–ga Yield of 3a–gb % eec
4a 9a, 71% 3a, 87% 94%
4b 9b, 92% 3b, 84% 87%
4c 9c, 73% 3c, 86% 92%
4d 9d, 93% 3d, 83% 96%
4e 9e, 77% 3e, 90% 96%
4f 9f, 82% 3f, 89% 95%
4g 9g, 84% 3g, 73% 96%
a

All reactions were performed on a 1.0 mmol scale.

b

All reactions were performed on a 0.5 mmol scale.

C

Enantiomeric excess determined by 19F NMR using the (R)-Mosher amide of the final amine.