Skip to main content
. Author manuscript; available in PMC: 2016 Feb 11.
Published in final edited form as: J Am Chem Soc. 2015 Jan 27;137(5):2042–2046. doi: 10.1021/ja512529e

Table 3.

Scope of aryl iodide reagents for the enantioselective arylation of cyclopropylmethylaminesa,b

graphic file with name nihms688013f4.jpg
a

Experiments were performed with 1 (0.2 mmol), aryl iodide (0.6 mmol), Pd(OAc)2 (0.02 mmol), Ag2CO3 (0.4 mmol), sodium trifluoroacetate (0.1 mmol), Boc-L-Val-OH (0.04 mmol) in t-BuOH (1 mL) for 18 hours at 80 ºC under air.

b

Isolated yields.