First synthesis of 1-deazacytidine, the C-nucleoside analogue of cytidine
The synthesis of 1-deazacytidine, the C-nucleoside analogue of cytidine, is described. It involves coupling of a protected 2-amino-5-bromopyridine with perbenzylated ribonolactone and transformation of the pyridine ring into the desired substituted pyridone. This synthesis completes the family of C-...
Main Authors: | Sollogoub, M, Fox, K, Powers, V, Brown, T |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2002
|
Similar Items
-
Combining nucleoside analogues to achieve recognition of oligopurine tracts by triplex-forming oligonucleotides at physiological pH.
by: Rusling, D, et al.
Published: (2005) -
Synthesis and O-phosphorylation of 3,3,4,4-tetrafluoroaryl-C-nucleoside analogues
by: Bonnac, L, et al.
Published: (2010) -
Synthesis and O-phosphorylation of 3,3,4,4-tetrafluoroaryl-C-nucleoside analogues.
by: Bonnac, L, et al.
Published: (2010) -
Recognition of CG inversions in DNA triple helices by methylated 3H-pyrrolo[2,3-d]pyrimidin-2(7H)-one nucleoside analogues.
by: Ranasinghe, RT, et al.
Published: (2005) -
Differential susceptibility of retroviruses to nucleoside analogues.
by: Rosenblum, L, et al.
Published: (2001)