Synthesis of novel hydroxymethyl substituted analogues related to carbovir and neplanocin A
Research output: Contribution to journal › Journal article › Research › peer-review
Two enantiomerically pure hydroxymethyl substituted cyclopentene nucleoside analogues (42 and 53) related to carbovir and neplanocin A, respectively, were prepared from the chiral pool of iridoid glucosides. In addition two saturated hydroxymethylated analogues (44 and 45) were obtained from a protected intermediate.
| Original language | English |
|---|---|
| Journal | Nucleosides, Nucleotides and Nucleic Acids |
| Volume | 21 |
| Issue number | 1 |
| Pages (from-to) | 23-43 |
| Number of pages | 21 |
| ISSN | 1525-7770 |
| DOIs | |
| Publication status | Published - 2002 |
| Externally published | Yes |
- Adenosine, Dideoxynucleosides, Nucleosides
Research areas
ID: 47258155