Synthesis of 5-Phenyl-2 (1H)-pyrimidinone Nucleosides

M Krečmerová, H Hřebabecký…

Index: Krecmerova, Marcela; Hrebabecky, Hubert; Masojidkova, Milena; Holy, Antonin Collection of Czechoslovak Chemical Communications, 1996 , vol. 61, # 3 p. 458 - 477

Full Text: HTML

Citation Number: 5

Abstract

Abstract Reaction of 2-phenyltrimethinium salt 1 with thiourea and subsequent reaction with chloroacetic acid afforded 5-phenyl-2 (1H)-pyrimidinone (3). Its silyl derivative 4 was condensed with 1-O-acetyl-2, 3, 5-tri-O-benzoyl-D-ribofuranose under catalysis with tin tetrachloride or trimethylsilyl trifluoromethanesulfonate to give protected nucleoside 5 together with 5', O 6-cyclo-5-phenyl-1, 3-bis-(β-D-ribofuranosyl)-6-hydroxy-5, 6-dihydro-2 ( ...

Related Articles:

Addition of C-nucleophiles to 5-phenylpyrimidin-2 (1H)-ones and 6-phenyl-1, 2, 4-triazin-3 (2H)-one

[Egorov, Ilya N.; Tseitler, Tatyana A.; Zyryanov, Grigory V.; Rusinov, Vladimir L.; Chupakhin, Oleg N. Arkivoc, 2011 , vol. 2011, # 10 p. 312 - 323]

More Articles...