Synthesis of Pyrimidine??Containing Nucleoside β??(R/S)??Hydroxyphosphonate Analogues
M Meurillon, L Chaloin, C Périgaud…
Index: Meurillon, Maia; Chaloin, Laurent; Perigaud, Christian; Peyrottes, Suzanne European Journal of Organic Chemistry, 2011 , # 20-21 p. 3794 - 3802
Full Text: HTML
Citation Number: 3
Abstract
Abstract A concise route to nucleoside β-hydroxyphosphonate analogues is described. The use of a nucleoside β-ketophosphonate as the key intermediate allowed both the (R) and (S) isomers of β-hydroxyphosphonate analogues in the pyrimidine series to be accessed. Such derivatives may be considered as stable mimics of 5′-monophosphate nucleosides and, therefore, could be the starting point for the development of potential therapeutic agents.
Related Articles:
[Giri; Prabhavathi Devi; Gangadhar; Narasimha Rao; Lingaiah; Sai Prasad; Prasad Synthetic Communications, 2006 , vol. 36, # 1 p. 7 - 11]
[Bulletin of the Chemical Society of Japan, , vol. 71, # 3 p. 723 - 734]
[Bulletin of the Chemical Society of Japan, , vol. 71, # 3 p. 723 - 734]
[Bulletin of the Chemical Society of Japan, , vol. 71, # 3 p. 723 - 734]
Iodide-catalyzed reductions: development of a synthesis of phenylacetic acids
[Milne, Jacqueline E.; Murry, Jerry A.; King, Anthony; Larsen, Robert D. Journal of Organic Chemistry, 2009 , vol. 74, # 1 p. 445 - 447]