4.4 Article

20-deoxy-20-fluorocamptothecin: Design and synthesis of camptothecin isostere

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SYNLETT
卷 -, 期 14, 页码 2509-2512

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GEORG THIEME VERLAG KG
DOI: 10.1055/s-2004-834810

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fluorine. antitumor agent; asymmetric synthesis; camptothecin; topoisomerase I

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20-Deoxy-20-fluorocamptothecin (2) has been synthesized as an isosteric analogue of camptothecin (1). The use of selectfluor or N-fluorobenzenesulfonimide for the electrophilic fluorination of 20-deoxycamptothecin (3) yields the target compound. Enantioselective fluorination of 3 was also achieved using our previously described cinchona alkaloids/selectfluor combination to provide both enantiomers of 2 with 88% ee and 81% ee, respectively.

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