Journal
SYNTHETIC COMMUNICATIONS
Volume 32, Issue 11, Pages 1757-1764Publisher
TAYLOR & FRANCIS INC
DOI: 10.1081/SCC-120004272
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N-glycosylation of 2,4-bis-O-(trimethylsilyl)-pyrimidine bases with 2-deoxy-2-fluoro-3,5-di-O-benzoyl-1-(Br, OBz)-alpha-D-arabinose derivatives are reported. I-Bromo-arabinose provides high yield and a favorable anomeric ratio (beta/alpha) of pyrimidine nucleoside in either MeCN or CH2Cl-CH2Cl. This method should be suitable for the synthesis of 2'-deoxy-2-[F-18]fluoro-1-beta-D-arabinofuranosyluracil derivatives.
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