112695-36-0Relevant articles and documents
Oxidation-reduction sequence for the synthesis of peracylated fluorodeoxy pentofuranosides
Mikhailopulo,Poopeiko,Sivets,Khripach
, p. 383 - 384 (1995)
Oxidation of 1a with DMSO-acetic or trifluoroacetic anhydride led to the formation of a mixture of epimeric gem-diols 2 and 3 in the ratios of ?3:1 and ?7:1, respectively. Reduction of this mixture with NaBH4 followed by benzoylation and chroma
Design and synthesis of A3 adenosine receptor ligands, 3′-fluoro analogues of Cl-IB-MECA
Kim, Hea Ok,Lim, Moo Hong,Park, Jae Gyu,Moon, Hyung Ryong,Jacobson, Kenneth A.,Kim, Hee-Doo,Chun, Moon Woo,Jeong, Lak Shin
, p. 923 - 925 (2007/10/03)
Synthesis of 3′-deoxy-3′-fluoro-N6-substituted adenosines as bioisosteres of Cl-IB-MECA and their binding affinities to A 3 adenosine receptor are described.
Synthesis and antiviral and cytostatic properties of 3'-deoxy-3'-fluoro- and 2'-azido-3'-fluoro-2',3'-dideoxy-D-ribofuranosides of natural heterocyclic bases
Mikhailopulo,Poopeiko,Pricota,Sivets,Kvasyuk,Balzarini,De Clercq
, p. 2195 - 2202 (2007/10/02)
A series of 3'-deoxy-3'-fluoro- and 2'-azido-2',3'-dideoxy-3'-fluoro-D-ribofuranosides of natural heterocyclic bases have been synthesized with the use of universal carbohydrate precursors, viz., 1-O-acetyl-2,5-di-O-benzoyl-3-deoxy-3-fluoro-D-ribofuranose