Skip to main content
. Author manuscript; available in PMC: 2014 Jun 26.
Published in final edited form as: Bioorg Med Chem. 2011 Feb 18;19(7):2287–2297. doi: 10.1016/j.bmc.2011.02.026

Figure 2a.

Figure 2a

HPLC analysis of a reaction between the OH-protected ClCF2-precursor (4, Approach A) with K18F/Kryptofix in DMF after heating at 150°C for 10 minutes. The analytical HPLC was performed using a C18 column and a mobile phase of acetonitrile and water (40/60) at a flow rate of 2 mL/min (for details see section 6.1. General Methods). Compound 4, which is a mixture of 2 diastereomers, appears as a double peak in the HPLC chromatogram. The major product of the reaction, which appears as a double peak at a retention time of approximately 5 min, is also a mixture of 2 diastereomers (see Scheme 1). (Vertical axes are in arbitrary units.)