164406-65-9Relevant articles and documents
An efficient method for the synthesis of aromatic C-nucleosides
Chaudhuri, Narayan C.,Kool, Eric T.
, p. 1795 - 1798 (1995)
Reaction of diarylcadmium or diarylzinc reagents with 1,2-dideoxy-3,5-di-O-p-toluoyl-1-chloro-α-D-ribofuranose affords 3,5-di-O-protected aromatic C-nucleosides in good yields.
Triphenylphosphine: A catalyst for the synthesis of C-aryl furanosides from furanosyl halides
Nicolas, Lionel,Angibaud, Patrick,Stansfield, Ian,Meerpoel, Lieven,Reymond, Sébastien,Cossy, Janine
supporting information, p. 849 - 852 (2014/02/14)
An array of C-aryl furanosides was prepared in good yields from furanosyl halides and aryl Grignard reagents in Et2O using PPh3 as a catalyst.