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The synthetic study of 2', 3'-diazido and difluoro secouridines toward development of new antiviral agents is discribed. These acyclic nucleosides were synthesized from uridine by the method of ring opening reaction of sugar moiety.
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An Efficient Synthesis of Cyclic $\alpha$, $\alpha$-Disubstituted $\alpha$-Amino Acids
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C-뉴크레오사이드의 화학합성
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