Abstract
Condensation of 5-aminocytidine with N-methylisatin yielded a new heterocyclic system, 8H,10H,15b(S)-2,3,6,7-tetrahydro-1,5,3-dioxazepino[3,2- c]indolo[3,2-g]pteridine-7-one. The assignment of S configuration at position 15b, which is generated as a result of the nucleophilic attack of the 5'- hydroxy of the ribosyl moiety at the position 6 of the cytosine base, is discussed.
| Original language | English |
|---|---|
| Pages (from-to) | 1701-1710 |
| Number of pages | 10 |
| Journal | Nucleosides and Nucleotides |
| Volume | 15 |
| Issue number | 11-12 |
| DOIs | |
| State | Published - 1996 |
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