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. Author manuscript; available in PMC: 2014 Nov 27.
Published in final edited form as: J Med Chem. 2013 Nov 11;56(22):9019–9030. doi: 10.1021/jm400894u

Scheme 1.

Scheme 1

Synthesis of 4.a

a. Alcohols Ia and Ib were prepared as a mixture of regioisomers (~3:1) by following a reported enantioselective synthesis (ref 12). The ratio of IIIa:IIIb was ~3:1. Amine llla was purified as the HCl salt. Ts, p-toluenesulfonyl; phth, phthalimide anion.