139871-31-1Relevant articles and documents
Methoxymethyl (MOM) group nitrogen protection of pyrimidines bearing C-6 acyclic side-chains
Kraljevic, Tatjana Gazivoda,Petrovic, Martina,Kristafor, Svjetlana,Makuc, Damjan,Plavec, Janez,Ross, Tobias L.,Ametamey, Simon M.,Raic-Malic, Silvana
, p. 5113 - 5129 (2011)
Novel N-methoxymethylated (MOM) pyrimidine (4-13) and pyrimidine-2,4- diones (15-17) nucleoside mimetics in which an isobutyl side-chain is attached at the C-6 position of the pyrimidine moiety were synthesized. Synthetic methods via O-persilylated or N-a
Syntheses and antitumor evaluation of C(6)-isobutyl- and C(6)-isobutenyl-substituted pyrimidines, and dihydropyrrolo[1,2-c]pyrimidine-1, 3-diones
Kristafor, Svjetlana,Kraljevic, Tatjana Gazivoda,Ametamey, Simon M.,Cetina, Mario,Ratkaj, Ivana,Hacek, Romana Tandara,Pavelic, Sandra Kraljevic,Raic-Malic, Silvana
, p. 1455 - 1469 (2011/11/05)
A growing body of evidence supports that pyrimidine derivatives, in which the sugar residues have been replaced by acyclic side chains, might be developed as promising anticancer agents that interfere with tumor cell proliferation, survival, and metastati
Synthesis of anti-restricted pyrimidine acyclic nucleosides
Hsu,Wise,Kucera,Drach,Townsend
, p. 3354 - 3358 (2007/10/02)
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