Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Ethyl phosphonate nucleosides with

The syntheses of carbocyclic analogs of phosphononucleosides (29) and (30a-c) have been reported. Phosphonic acid (29) was obtained by introduction of the benzoylated thymine on the 2(4-hydroxycyclopent-2-enyl)ethyl phosphonic acid diisopropyl ester under Mitsunobu conditions while (30a-c) were prepared by building-up the base around a phosphono-cyclopentylamine moi-ety. The vinylphosphonate derivatives of uridine, cytidine and cytosine ara-binoside (31a-c) have been prepared by Wittig condensation of [(diethoxyphos-phinyl)methylidene]triphenylphosphorane with the appropriately protected 5-aldehydic nucleoside derivatives. Dihydroxylation of the novel vinyl phosphon-ates offered the dihydroxylated phosphonate derivatives (32a-c). Each of these novel compounds was evaluated as substrates for the enzyme nucleotide monophosphate kinase, and their toxicity to K562 cells. All analogues were found to be poorly phosphorylated by the kinase and exhibited poor in vivo toxicity. ... [Pg.169]

Synthesis of the modified triphosphate subunit was accomplished starting from ethyl bis(bromomethyl)phosphinate 253 (Scheme 51). An Arbusov reaction with triethyl phosphite and trimethyl phosphite, respectively, produced bis (phosphonomethyl)phosphjnate 255 in 40% overall yield. A selective monodemethylation by cyanide and acidificaticHi led to monophosphonic acid 256. Bismethylene triphosphate (BMT) 258 analogues of nucleosides were obtained by coupling of the 5 -free OH nucleosides 257 with phosphonate 256 under Mitsunobu conditions [181,182]. TMSBr mediated deprotection followed by treatment with aqueous anmumia and cation exchange afforded bismethylene analogues 259 of nucleoside triphosphate in yields up to 62%. [Pg.93]

Nucleosides. Nucleotides, and Derivatives.- 2, 3 ,5 -Trl-0 -acetyl-adenosine and -guanosine, 4- -ethyl-thymidlne, N -methyl-2 -deoxyadenoslne, 5-raethoxymethyl-2 -deoxy-urldlne and its 0-D-threo-isomer, 5-fluoroarablnosylcytoslne, the 2 -deoxynucleo-side (17), cls-thymldine 3 ,5 -cyclic methyl phosphonate and the corresponding 3, 5 -cycllc N,N-dlmethylphosphoramldate,a cobalt(II) complex with 2 -deoxyinosine 5 -monophosphate,... [Pg.241]


See other pages where Ethyl phosphonate nucleosides with is mentioned: [Pg.167]    [Pg.220]    [Pg.212]    [Pg.185]    [Pg.242]    [Pg.216]    [Pg.130]    [Pg.122]    [Pg.186]    [Pg.170]    [Pg.69]   
See also in sourсe #XX -- [ Pg.49 ]




SEARCH



Ethyl phosphonate

Nucleoside phosphonates Nucleosides

© 2024 chempedia.info