Enantiomeric Synthesis of L-(or 1'R,2'S)-Carbocyclic Cyclopropyl Nucleosides. -The title compounds (VII), (X), (XIII), and (XVI) are prepared in order to test their biological activity. -(LEE, M.
Enantiomeric Synthesis of l -(or 1‘ R ,2‘ S )-Carbocyclic Cyclopropyl Nucleosides
✍ Scribed by Lee, Mi Gyoung; Du, Jin Fa; Chun, Moon Woon; Chu, Chung K.
- Book ID
- 120991913
- Publisher
- American Chemical Society
- Year
- 1997
- Tongue
- English
- Weight
- 207 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0022-3263
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📜 SIMILAR VOLUMES
The total synthesis of L-(or IS,2R,3S,5S)-bicarbocyclic nucleosides (8-15) has been accomplished. The key intermediate 3 was synthesized in two steps from the known chiral compound 1 through a stereoselective cyclopropanation under Furukawa conditions and its X-ray structure has been determined. The
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