933995-41-6Relevant 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.
Pyrrolo[2,3-d]pyrimidine β-L-nucleosides containing 7-deazaadenine, 2-amino-7-deazaadenine, 7-deazaguanine, 7-deazaisoguanine, and 7-deazaxanthine
Seela, Frank,Peng, Xiaohua
, p. 956 - 977 (2008/02/10)
The synthesis and properties of 7-deazapurine β-L-nucleosides are described. The stereoselective glycosylation of the anions of 2-amino-6-chloro-7-deazapurines 9a, 9b or 6-chloro-7-deazapurines 13a, 13d with 3,5-di-O-(4-methylbenzoyl)-2-deoxy-α-L-erythro-
