82018-89-1Relevant articles and documents
SYNTHESIS OF THE RIBOSIDE ANALOG OF THE PYRIMIDINE ADDUCT FORMED IN THE REACTION BETWEEN THE CARCINOGEN N-HYDROXY-N-2 ACETYLAMINOFLUORENE AND DNA
Robillard, B.,Lhomme, M. F.,Lhomme, J.
, p. 2659 - 2662 (1985)
A general synthesis has been achieved to obtain carcinogen modified guanosines.The method was applied to the preparation of the N-2,5-diamino-4-oxo-3H-pyrimidine-6-yl-N-(β-D-ribofuranosyl)-N'-(2-fluorenyl)urea 6.