Synthesis of anhydro psicofuranosyl nucleosides
✍ Scribed by Jarkko Roivainen; Jouko Vepsäläinen; Alex Azhayev; Igor A. Mikhailopulo
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 74 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Recent studies from this laboratory have shown that 6,5'-cyclopyrlmidine nucleosides2, for example the isopropylideneuridine analogue 1, are very susceptible to oxidation at C-5'. Thus, autoxidation3 of 1. with 02-NaOH, or treatment with Mn02 in methanol readily affords the 5'-ketonucleoside 4. The
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v