Chemical synthesis of nucleoside analogues
I tiakina i:
| Kaituhi rangatōpū: | |
|---|---|
| Ētahi atu kaituhi: | |
| Hōputu: | Tāhiko īPukapuka |
| Reo: | Ingarihi |
| I whakaputaina: |
Hoboken, N.J. :
Wiley,
c2013.
|
| Ngā marau: | |
| Urunga tuihono: | An electronic book accessible through the World Wide Web; click to view |
| Ngā Tūtohu: |
Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!
|
Rārangi ihirangi:
- Deoxynucleoside analogues / Vicente Gotor
- Nucleosides modified at the base moiety / Luigi Agrofoglio
- Acyclic nucleosides / Antonin Holy
- Phosphorylated nucleoside analogues / Giovanni Romeo
- Triphosphorylated nucleoside analogues / Chris Meier
- Pro-nucleotides / Christian Perigaud
- C-nucleoside / Sergio Castillón
- Isonucleosides / Vasu Nair
- Conformationally constrained nucleosides / Jacques Lebreton
- Spironucleosides / Maria Jose Camarasa
- L-nucleosides / Daniela Perrone
- Carbocyclic nucleosides / Eric Leclerc
- Uncommon three-, four, and six-membered nucleosides / Elisabetta Groaz
- Thionucleosides / L.S. Jeong
- Azanucleosides and related compounds / Tomas Tejero
- Oxathiolane and dioxolane nucleosides / Annalisa Guaragna
- Isoxazolidinyl nucleosides / Ugo Chiacchio
- Nucleoside antibiotics / Apurba Dutta
- Building blocks for peptide nucleic acids / Pedro Merino.