Diastereoselective Synthesis of C2′-Fluorinated Nucleoside Analogues Using an Acyclic Approach
journal contributionposted on 13.10.2016, 00:00 by Starr Dostie, Michel Prévost, Philippe Mochirian, Kashif Tanveer, Nicholas Andrella, Ariana Rostami, Guillaume Tambutet, Yvan Guindon
Nucleoside analogues bearing a fluorine in the C2′-position have been synthesized by SN2-like cyclizations of acyclic thioaminal precursors. This strategy provides access to two scaffolds, d-1′,2′-cis-thiofuranosides and d-1′,2′-trans-furanosides, which are difficult to generate using the standard approach for nucleoside synthesis. The addition of silylated nucleobases onto model C2-fluorinated dithioacetal substrates resulted in 1,2-syn diastereoselectivity, which is consistent with the C2–F and S-alkyl moiety being in close proximity. A new series of analogues bearing a C3′ all-carbon quaternary center along with a C2′–F atom have also been synthesized using this approach and are being investigated as potential antimetabolites.
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ciseriesdiastereoselectivityS N 2-Diastereoselective Synthesisfluorinesilylated nucleobasesproximityAcyclic Approach Nucleoside analoguesscaffoldcyclizationthiofuranosidestrategyaccessapproachalkyl moietyacyclic thioaminal precursorsmodel C 2-fluorinated dithioacetal substratesall-carbonnucleoside synthesisfuranosidecentertranantimetabolitequaternaryAnalogue