115747-35-8Relevant articles and documents
Chemical synthesis of 2′-deoxyguanosine-C8 adducts with heterocyclic amines: An application to synthesis of oligonucleotides site-specifically adducted with 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine
Takamura-Enya, Takeji,Ishikawa, Satoko,Mochizuki, Masataka,Wakabayashi, Keiji
, p. 770 - 778 (2007/10/03)
Synthesis of 2′-deoxyguanosine-C8 adducts (dG-C8 adducts) with mutagenic/carcinogenic heterocyclic amines (HCAs) was achieved via the Buchwald-Hartwig arylamination reaction. By using tris-(dibenzylideneacetone) dipalladium (Pd2dba3)
Synthesis of the C8-deoxyguanosine adduct of the food mutagen IQ.
Wang,Rizzo
, p. 565 - 568 (2007/10/03)
[structure: see text] The C8-2'-deoxyguanosine adduct of the food mutagen 2-amino-3-methylimadazo[4,5-f]-quinoline (IQ) has been synthesized. The key step is a palladium-catalyzed N-arylation of a suitably protected 8-bromo-2'-deoxyguanosine derivative.