2627-62-5Relevant articles and documents
Deoxygenative [1,2]-hydride shift rearrangements in nucleoside and sugar chemistry: Analogy with the [1,2]-electron shift in the deoxygenation of ribonucleotides by ribonucleotide reductases
Robins, Morris J.,Nowak, Ireneusz,Wnuk, Stanislaw F.,Hansske, Fritz,Madej, Danuta
, p. 8216 - 8221 (2008/03/15)
(Chemical Equation Presented) A variant of the semipinacol rearrangement that was observed in our laboratory has been applied to the synthesis of several furanose and pyranose derivatives. The process consists of an "orchestrated" [1,2]-hydride shift with
Synthesis of 2'-substituted derivatives of neplanocin A (nucleosides and nucleotides. XLIV)
Fukukawa,Uedao,Hirano
, p. 1582 - 1592 (2007/10/02)
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Nucleic acid related compounds.22. Transformation of ribonucleoside 2,3'-O-ortho esters into halo, deoxy, and epoxy sugar nucleosides using acyl halides. Mechanism and structure of products.
Robins,Mengel,Jones,Fouron
, p. 8204 - 8213 (2007/10/04)
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