873792-65-5Relevant academic research and scientific papers
An efficient synthesis of 7-functionalized 7-deazapurine β-D- or β-L-ribonucleosides: Glycosylation of pyrrolo[2,3-d]pyrimidines with 1-O-acetyl-2,3,5-tri-o-benzoyl-D-or L-ribofuranose
Peng, Xiaohua,Seela, Frank
, p. 603 - 606 (2008/03/14)
The glycosylation reaction performed with 7-halogenated 7-deazapurines employing commercially available 1-O-acetyl-2,3,5-tri-O-benzoyl-D- or L-ribofuranoses is described. Copyright Taylor & Francis Group, LLC.
7-Functionalized 7-deazapurine ribonucleosides related to 2-aminoadenosine, guanosine, and xanthosine: Glycosylation of pyrrolo[2,3-d]pyrimidines with 1-O-acetyl-2,3,5-tri-O-benzoyl-D-ribofuranose
Seela, Frank,Peng, Xiaohua
, p. 81 - 90 (2007/10/03)
The Silyl-Hilbert-Johnson reaction as well as the nucleobase-anion glycosylation of a series of 7-deazapurines has been investigated, and the 7-functionalized 7-deazapurine ribonucleosides were prepared. Glycosylation of the 7-halogenated 6-chloro-2-pival
