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Fig 1.

Chemical structures of 2’-deoxy-2’-[18F]fluoro-β-D-arbiofuranosylcytosine ([18F]FAC) and its analogs.

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Fig 2.

Classical synthesis of [18F]FAC employing HBr for activation and coupling to the cytosine silylether developed by Radu’s group.

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Fig 3.

Synthetic scheme for the synthesis of [18F]FAC using TMSOTf assisted coupling of 1.3.5-tribenzoyl-2-deoxy-2-[18F]fluoro-arabinofuranose with cytosine silyl ether using microwave heating.

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Fig 4.

a) HPLC chromatogram showing the purification of [18F]FAC using a semi preparative HPLC system. Blue line: radioactive signal from radioactive detector Red line: UV signal from UV detector @ 254 nm. b) Quality control analysis of [18F]FAC with analytical HPLC system showing coinjection of purified [18F]FAC from preparatory column and non-radioactive FAC.

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