116002-29-0Relevant academic research and scientific papers
122. Xylose-DNA containing the four natural bases
Seela, Frank,Heckel, Maximilian,Rosemeyer, Helmut
, p. 1451 - 1461 (1996)
Oligonucleotides containing (′-deoxy-β-D-xylofuranosyl)guanine have been prepared. For this purpose 2-aminoadenosine (5) was synthesized and converted to 2′-deoxy-β-D-xyloguanosine (1) The related 2′-deoxy-β-D-xyloisoguanosine (3) and 2′-deoxy-β-D-xyloxan
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
Nucleic acid related compounds. 57. Synthesis, X-ray crystal structure, lipophilic partition properties, and antiretroviral activities of anomeric 3'-azido-2',3'-dideoxy-2,6-diaminopurine ribosides
Robins,Wood,Dalley,Herdewijn,Balzarini,De Clercq
, p. 1763 - 1768 (2007/10/02)
Trimethylsilyl triflate-catalyzed transfer glycosylation of 2,6-diacetamidopurine (2) with 3'-azido-3'-deoxythymidine (AZT, 1) as donor followed by deprotection gave 2,6-diamino-9-(3-azido-2,3-dideoxy-α- and -β-D-erythro-pentofuranosyl)purines (3 and 4) i
