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2 -deoxyuridine

Application of this reaction to 2, 2-anhydrouridine (LXXXVII) led to a 3-substituted nucleoside (CIV) which, upon acylation followed by reduction with Raney nickel, yielded 3-deoxyuridine (CV, R = uracilyl). Reductive cleavage of CV, by the sodium-liquid ammonia procedure,72 afforded 3-deoxy-D-en/fAro-pentose ( 3-deoxy-D-ribose ), a result which establishes position 3 as the site originally containing the ethylthio function. The authors suggest,248 as a plausible route to CIV, the initial formation of the anion CII, followed by formation of the 2,3-anhydride structure. The anhydride (CIII) is then attacked, at C3, by the ethanethiol ion, to yield... [Pg.349]

Diazotization of 5-amino-3 -deoxyuridine 231 gave the 5-diazopyrimidooxazocine 232 through a nucleophilic attack of the C-5 oxygen on the electron-deficient C-4 carbon (Scheme 48) <2002W032920>. [Pg.217]

H2O), pKgst 9.3. 3 -Deoxyuridine is recrystallised from Me2CO/MeOH and is dried in a vacuum. [Michelson Todd / Chem Soc 816 7955.]... [Pg.676]

The common structural skeleton of the uridyl peptide antibiotics, the (25,35)-diaminobutyric acid (DABA) residue, serves as a connection point for the 3 -deoxyuridine moiety via a 4, 5 -enamide linkage. The DABA residue is acylated on both nitrogen substituents by peptide chains. [Pg.609]

Deoxy 3 -Deoxy-5-flnoroitridine. 5-Fluoro-3 -deoxyuridine CgHiiFNjOs 246.195 Cryst. (EtOH). Mp 169-171°. 5 -Phosphate [796-66-7]... [Pg.447]

Deoxyuridine, Z-3 2 -Deoxy- j/-uridine, D-354 2 -Deoxyuridine, D-382 3 -Deoxyuridine, D-383 5 -Deoxyuridine, D-384 2 -Deoxyuridine-5 -carboxamide, D-382 2 -Deoxyuridine-5 -carboxylic acid, D-382 2"-Deoxy-5 -uridylic acid, D-382 2 -Deoxy-5-vinyluridine, V-21... [Pg.1032]

C-Fluoroadenosine 5 -sulfamate, N-84 2-Fluoroadenosine, F-11 8-Fluoroadenosine, F-12 Fluoroancitabine, F-19 Fluoroblasticidin S, B-39 5-Fluorocytidine, F-13 p-Fluoro-ddA, L-48 2 -Fluoro-2 -deoxyadenosine, D-63 5-Fluoro-3 -deoxycytidine, F-13 5-Fluoro-3 -deoxyuridine, F-18 8-Fluoroerythromycin, E-18 5-C-Fluorogalactosyl fluoride, F-14... [Pg.1047]

Process of 3 -fluoro-3 -deoxyuridine (3 -F-3 -dUrd) phosphorolysis was analyzed in the presence of mutPyrNPase 2.5 U of enzyme activity were added to 3 -F-3 -dUrd in 2 mM PPB and the reaction was performed at 80°C with regular monitoring of phosphorolysis degree in the course of 96 h. [Pg.267]


See other pages where 2 -deoxyuridine is mentioned: [Pg.528]    [Pg.290]    [Pg.253]    [Pg.353]    [Pg.478]    [Pg.478]    [Pg.334]    [Pg.350]    [Pg.86]    [Pg.200]    [Pg.2038]    [Pg.528]    [Pg.676]    [Pg.180]    [Pg.141]    [Pg.872]    [Pg.872]    [Pg.187]    [Pg.157]    [Pg.264]    [Pg.143]    [Pg.273]   
See also in sourсe #XX -- [ Pg.290 ]




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2 -Amino-2 -deoxyuridine

2 -Deoxyuridine 5 -monophosphate

2 -Deoxyuridine 6-substituted 2 -deoxyuridines

2 -Deoxyuridine, structure

2-Deoxyuridine-5 -carboxylic acid

2-Deoxyuridines, synthesis

3-Methyl-2 -deoxyuridine

5 - - 2 -deoxyuridines -triphosphate

5- Trifluoromethyl- 2 -deoxyuridine

5-Bromo-2 -deoxyuridine

5-Deoxyuridine fluoro-, prodrugs

5-Ethynyl-2 -deoxyuridine

5-Fluoro-2 -deoxyuridine monophosphate

5-Fluoro-2 -deoxyuridine monophosphate FdUMP)

5-Fluoro-2 -deoxyuridine-5 -phosphate

5-Iodo-2 -deoxyuridine

5-formyl-2 -deoxyuridine

Chloro-deoxyuridine

DUMP (2*-deoxyuridine

Deoxyuridine 5’ triphosphate

Deoxyuridine diphosphate

Deoxyuridine from deoxycytidine

Deoxyuridine kinase

Deoxyuridine metabolism

Deoxyuridine monophosphate (dUMP

Deoxyuridine monophosphate, conversion

Deoxyuridine phosphates

Deoxyuridine phosphates formation

Deoxyuridine phosphorylation

Deoxyuridine suppression

Deoxyuridine suppression test

Deoxyuridine thymidine

Deoxyuridine-l’yl radical

Dibromovinyl deoxyuridines

Difluoro -2 -deoxyuridine

Disodium phosphate, 2 -deoxyuridine

Fluoro-deoxyuridine

Radicals deoxyuridin

Spectra deoxyuridine

Thymidine deoxyuridine effect

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