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. Author manuscript; available in PMC: 2014 Aug 16.
Published in final edited form as: Org Lett. 2003 Oct 30;5(22):4125–4127. doi: 10.1021/ol035773h

Figure 2.

Figure 2

Racemic tricycle 1 was acylated with 4-pentenoyl-(R,R)-pseudoephedrine, yielding diastereomers that were purified using silica gel chromatography. Following saponification, the resolved acids (+)-4 and (−)-4 were used in subsequent experiments.