118674-75-2Relevant articles and documents
C-GLYCOSYLATION OF SUBSTITUTED HETEROCYCLES UNDER FRIEDEL-CRAFTS CONDITIONS (I): A TWO-STEP SYNTHESIS OF THE THIENOPYRIMIDINE c-NUCLEOSIDE ANALOG OF INOSINE.
Rao, Sunkada P.,Rao, Kambhampati V. B.,Otter, Brian A.,Klein, Robert S.,Ren, Wu-Yun
, p. 3537 - 3540 (2007/10/02)
Direct stannic chloride catalyzed C-glycosylation of N-formyl-4-amino-3-carboalkoxy thiophenes with 1-O-acetyl-O-benzoyl-β-D-ribofuranose, followed by annelation of a fused pyrimidone ring upon treatment with ammonia, constitutes a short approach to the synthesis of a new C-nucleoside inosine analog.